TH97795A

TH97795A - Anthranilic diamide derivatives with hetero-aromatic and heterocyclic structural agents.

Info

Publication number: TH97795A
Application number: TH701002881A
Authority: TH
Inventors: อาคิม เฮนเซ่ ดร; โอลก้า มัลซัม ดร; ฟังเก้ ดรคริสเตียน; อาร์โนลด์ ดรคริสเตียน; วาดะ ดรคัตสึอากิ; เอลิก ดรเบิร์นด; วิลเฮล์ม ดรูวีส ดรมาร์ค; ฟิสเชอร์ ดรรูดิเจอร์; เฮนเซ่ ดรอาคิม; ซันวอลด์ ดรอีริช; มัลซัม ดรโอลก้า; มูราตะ นายเทตสึยะ; จอร์เกนส์ นายอูลริช; ดรเอิร์นท รูดอล์ฟ เอฟเจซิง ศาสตราจารย์
Original assignee: นางดารานีย์ วัจนะวุฒิวงศ์; นางสาวสนธยา สังขพงศ์; นางสาวสุคนธ์ทิพย์ จิตมงคลทอง; เบเยอร์ คร็อปไซเอนซ์ อัคเตียนเกเซลล์ชาฟท์
Filing date: 2007-06-11
Publication date: 2009-08-20

Abstract

DC60 (06/09/50) การประดิษฐ์นี้เกี่ยวข้องกับยาฆ่าแมลงชนิดใหม่ที่มีสูตรโครงสร้าง (I) (สูตรเคมี) (I) โดยที่ R1, R2, R3, R4, R5, R7, A, Q, และ n สามารถมีนิยามดังที่กล่าวไว้แล้วในคำอธิบาย, เกี่ยวข้อง กับกระบวนการจำนวนหนึ่งสำหรับการเตรียมสารเหล่านี้, เกี่ยวข้องกับการใช้สารประกอบเหล่านี้ในรูปของ สารประกอบออกฤทธิ์, และเกี่ยวข้องโดยเฉพาะกับการใช้สารเหล่านี้ในรูปขององค์ประกอบที่ใช้ควบคุมแมลง รบกวน การประดิษฐ์นี้เกี่ยวข้องกับยาฆ่าแมลงชนิดใหม่ที่มีสูตรโครงสร้าง (I) (สูตรเคมี) (I) โดยที่ R1, R2, R3, R4, R5, R7, A, Q, และ n สามารถมีนิยามดังที่กล่าวไว้แล้วในคำอธิบาย, เกี่ยวข้อง กับกระบวนการจำนวนหนึ่งสำหรับการเตรียมสารเหล่านี้, เกี่ยวข้องกับการใช้สารประกอบเหล่านี้ในรูปของ สารประกอบออกฤทธิ์, และเกี่ยวข้องโดยเฉพาะกับการใช้สารเหล่านี้ในรูปขององค์ประกอบที่ใช้ควบคุมแมลง รบกวนDC60 (06/09/50) This invention relates to a novel insecticide with structural formula (I) (chemical formula) (I), where R1, R2, R3, R4, R5, R7, A, Q, and n can be defined as described in the description; involves a number of processes for their preparation; involves the use of these compounds in the form of active compounds; and specifically involves the use of these compounds as components for controlling insect pests. This invention relates to a novel insecticide with structural formula (I) (chemical formula) (I), where R1, R2, R3, R4, R5, R7, A, Q, and n can be defined as described in the description; involves a number of processes for their preparation; involves the use of these compounds in the form of active compounds; and specifically involves the use of these compounds as components for controlling insect pests.

Claims

Revised 23/05/2016 1. Compounds of formula (I) (I) (chemical formula) where R1 represents hydrogen, amino, or hydroxyl, or represents C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each of which is not substituted, or is substituted once or more by identical or different substituents which can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, (C1-C4 alkoxy) carbonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, or (C1-C4 alkyl)C3-C6 cycloalkylamino, R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxycarbonyl, or C2-C6 alkylcarbonyl. R3 represents hydrogen, or represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, C3-C12 cycloalkyl, C3-C12 cycloalkyl-C1-C6 alkyl, and C4-C12 bisocloalkyl, each of which may... Choose to replace one or more substitute groups with similar or different ones that can be selected. Obtained independently from halogens, cyano, nitro, hydroxyl, amino, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoximino, C1-C4 alkylsulfoximino-C1-C4 alkyl, C1-C4 alkylsulfoximino-C2-C5 alkylcarbonyl, C2-C6 alkoxycarbonyl. C2-C6 alkyl carbonyls, C3-C6 trialkylsilyls, or 5 or 6-membered heteroaromatic rings, R2 and R3 can be bonded to each other via two to six carbon atoms and form a ring which is further, as appropriate, added with nitrogen, sulfur, or oxygen atoms, and which, as appropriate, may be replaced one to four times with C1-C2 alkyl, halogen, cyano, amino, or C1-C2 alkoxy. R2 and R3 together also replace... =S(C1-C4 alkyl)2 or =S(O)(C1-C4 alkyl)2 R4 represents hydrogen, halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkyl-thio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino. C3-C6 cycloalkylamino, (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl, or two R4s fused through an adjacent carbon atom may form a ring which replaces -(CH2)3-, -(CH2)4-,-(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)-, or -(CH=CH-N=CH)-, or two R4s fused through an adjacent carbon atom, forming the following fused ring, which, as appropriate, is replaced by one or More often by identical or different substituent groups that can be independently selected from hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C3-C6 halocycloalkyl, halogen, C1-C6 alkoxy, C1-C4 alkylthio(C1-C6 alkyl), C1-C4 alkylsulfide. C1-C6 alkyl, C1-C4 alkylsulfonyl(C1-C6 alkyl), C1-C4 alkylamino, di(C1-C4 alkyl)amino, or C3-C6 cycloalkylamino (chemical formula). n represents 0 to 3. R5 represents C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C1-C6 halocycloalkyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkinyl, C2-C6 haloalkinyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl. C1-C4 haloalkylthio, C1-C4 haloalkylsulfonil, C1-C4 haloalkylsulfonil, halogen, cyano, nitro, or C3-C6 trialkylsilyl, R6 replaces hydrogen, C1-C6 alkyl, C2-C6 alkynil, C2-C6 alkynil, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinil, or (chemical formula) R7 in each case, independently, replaces hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfonil, or C1-C4 haloalkylthio, M represents 0 to 4, X represents N, CH, CF, CCl, CBr, or CI, A represents –CH2-, CH(CH)3C(CH3)2, or CH2CH2, Q represents a 5- or 6-membered heteroaromatic ring or an 8, 9, or 10-membered heterobicyclic ring system fused with an aromatic type, an unreplaced ring system, or one or more replacements with identical or different substituents that can be selected. Free from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 al-kinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkyl sulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, or Q also represents a 5- or 6-membered heteroaromatic or heterocyclic ring system, or an 8, 9, or 10-membered aromatic fused heterocyclic ring system, where this ring or ring system is either unreplaced or replaced once or more by identical or different substituents that can be independently selected from hydrogen, C1-C6 alkyl, C2-C6 alkynyl. C2-C6 alkynil, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinil, C2-C6 haloalky-nil, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinil, C1-C4 alkylsulfonil, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinil, C1-C4 haloalkylsulfonil, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino. (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, or independently selectable substituents from phenyls or 5 or 6-membered heteroaromatic rings, which are possible for this phenyl or ring that is unsubstituted or substituted once or more, either the same or different from substituents of the types C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3- 2. Compounds of formula (I) according to claim 1, where R1 represents hydrogen, amino, or hydroxyl, or C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each of which is unsubstituted or substituted once or more by identical or different substituents which can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, (C1-C4 alkoxy)carbonyl, C1-C4 alkylamino, Di(C1-C4 alkyl)amino, C3-C6 cycloalkyl-amino, or (C1-C4 alkyl)C3-C6 cycloalkylamino. R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxy-carbonyl, or C2-C6 alkylcarbonyl. R3 represents hydrogen, or represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, each of which may be replaced once or... Furthermore, they are composed of similar or different substituent groups that can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthione, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoxymino, C1-C4 alkylsulfoxymino-C1-C4 alkyl, C1-C4 alkylsulfoxymino-C2-C5 alkylcarbonyl. C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, or C3-C6 trialkylsilyl, R4 replaces hydrogen, halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino. Two C3-C6 cycloalkylamino, (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl R4 molecules, formed by passing through adjacent carbon atoms, may form a ring representing -(CH2)3-, -(CH2)4-,-(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)-, or -(CH=CH-N=CH)-, where n represents 0 to 3, and R5 represents C1-C6 alkyl, C3-C6 cycloalkyl. C1-C6 haloalkyl, C1-C6 halocycloalkyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, halogen, cyano, nitro, or C3-C6 trialkylcylyl (R6 replaces hydrogen), C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl. C1-C6 haloalkyl, C2-C6 haloalkinyl, or (chemical formula) R7, in each case independently, represents hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkylthio. m represents 0 to 4. X represents N, CH, CF, CCl, CBr, or CI. A represents -CH2-, -CH(CH3)C(CH3)2-, or -CH2CH2. Q represents a 5- or 6-membered heteroaromatic ring or an 8-, 9-, or 10-membered heterobicyclic ring system fused to an aromatic type. This ring system is not replaceable, or can be replaced once or more by identical or different substitute groups that can be selected. Free from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 al-kinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkyl sulfenyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfenyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino or salts of these substances. 3. Compounds of the formula (I-1) (I-1) (chemical formula) where R1 represents hydrogen, R2 represents hydrogen, R3 represents C1-C4 alkyl, R4 represents hydrogen, methyl, trifluoromethyl, cyano, fluorine, chlorine, bromine, iodine or trifluoromethoxy, R5 represents methyl, Fluorine, chlorine, bromine, or iodine. R6 represents fluorine, chlorine, or bromine. X represents N, CCl4, or CH3. A represents CH2, CH(CH3). Q represents the aromatic heterocyclic ring of the Q-37, Q-38, Q-39, Q-40, Q-58, and Q-59 series, which may be selected as a substituent at a single or multiple positions in the structure. It also represents the 5-membered heterocyclic ring system Q-60, where these substituents can be independently selected from C1-C3 alkyl, C1-C3 haloalkyl, C1-C2 alkoxy, halogen, cyano, hydroxyl, nitro, or C1-C2 haloalkoxy, or these substituents can be independently selected from phenyl, or 5 or 6-membered heteroaromatic rings. Possible substituents include phenyl or other rings substituted at specific positions. The appropriate structure, one or more times, by different or similar substituent groups: C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, NO2, C1-C4 alkoxy or C1-C4 haloalkoxy or salts of these; 4. A method for controlling phytopathogenic fungi, which includes the use of compounds of Reservation 1; 5. A method for controlling phytopathogenic fungi, which includes the action of compounds of formulation (I) of Reservation 1 on phytopathogenic fungi; 6. A process for the production of agricultural chemical compounds, which includes the use of 7. A method for the treatment of phytopathogenic fungi consisting of the use of the compounds of formulation (I) according to claim 1. 8. Seeds treated with the compounds of formulation (I) according to claim 1. 9. A process for the production of an agricultural chemical compound consisting of the mixing of the compounds of formulation (I) according to claim 2 with additional substances and/or surface-active substances. 10. A method for the treatment of phytopathogenic fungi consisting of the use of the compounds of formulation (I) according to claim 2. 11. Seeds treated with the compounds of formulation (I) according to claim 2. 12. A method for the control of phytopathogenic fungi consisting of the use of the compounds of formulation (I) according to claim 2. Claim 2 13. The process of preparing compounds of formula (I) according to Claim 1 which includes (A) the aniline reaction of formula (II) (II) (chemical formula) in which A, R1, R2, R3, R4, R5 are defined by formula I with carbonyl chloride of formula (III) (III) (chemical formula) in which R6, A and Q are defined by formula I in the presence of an acid crosslinking agent; (B) the aniline reaction of formula (II) (II) (chemical formula) in which A, R1, R2, R3, R4, R5 are defined by formula I with carbonyl chloride of formula (IV) (IV) (chemical formula) in which R6, A and Q are defined by formula I in the presence of a condensing agent; or (C) the synthesis of anthnaamide of formula (I) in which R1 is replaced by hydrogen by the reaction Benzosacinone reaction of formula (V) (V) (chemical formula) where R4, R5, R6, A, Q and n are defined by formula I with amines of formula (XV) (XV) (chemical formula) where R2 and R3 are defined by formula I in the presence of dilutions 14. Compounds of formula (I) (I) (chemical formula) where R1 replaces hydrogen, amino, or hydroxyl or replaces C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each of which is unsubstituted or substituted once or more by identical or different substituents which can be independently selected from halogens, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, (C1-C4 alkoxy) carbonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino or (C1-C4 alkyl)C3-C6 cycloalkylamino, R2 replaces hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxy carbonyl or C2-C6 alkyl carbonyl, R3 replaces hydrogen or replaces C1-C6 alkyl, C1-C6 alkoxy. C2-C6 alkynyl, C2-C6 alkynyl, C3-C12 cycloalkyl, C3-C12 cycloalkyl-C1-C6 alkyl, and C4-C12 bisocloalkyl, each of which may be selectively replaced once or more times with identical or different substituents. They are obtained independently from halogens, cyano, nitro, hydroxyl, amino, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoximino, C1-C4 alkylsulfoximino-C1-C4 alkyl, C1-C4 alkylsulfoximino-C2-C5 alkylcarbonyl, C2-C6 alkoxycarbonyl. C2-C6 alkyl carbonyls, C3-C6 trialkylsilyls, or 5 or 6-membered heteroaromatic rings, R2 and R3 can be bonded to each other via two to six carbon atoms and form a ring which is further, as appropriate, added with nitrogen, sulfur, or oxygen atoms, and which, as appropriate, may be replaced one to four times with C1-C2 alkyl, halogen, cyano, amino, or C1-C2 alkoxy. R2 and R3 together also replace... =S(C1-C4 alkyl)2 or =S(O)(C1-C4 alkyl)2 R4 represents hydrogen, halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkyl-thio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino. C3-C6 cycloalkylamino, (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl, or two R4s fused through an adjacent carbon atom may form a ring which replaces -(CH2)3-, -(CH2)4-,-(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)-, or -(CH=CH-N=CH)-, or two R4s fused through an adjacent carbon atom, forming the following fused ring, which, as appropriate, is replaced once or More specifically, by identical or different substituent groups that can be independently selected from hydrogen, C1-C6 alkyls, C3-C6 cycloalkyls, C1-C6 haloalkyls, C3-C6 halocycloalkyls, halogens, C1-C6 alkoxys, C1-C4 alkylthio(C1-C6 alkyls), C1-C4 alkylsulfinyl(C1-C6 alkyls), C1-C4 alkylsulfonyl(C1-C6 alkyls), C1-C4 alkylaminos, di(C1-C4 alkyl)aminos, or C3-C6 cycloalkylaminos (chemical formulas). n represents 0 to 3, R5 represents C1-C6 alkyls, C3-C6 cycloalkyls, C1-C6 haloalkyls, C1-C6 halocycloalkyls. C2-C6 alkynil, C2-C6 haloalkinil, C2-C6 alkynil, C2-C6 haloalkinil, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinil, C1-C4 alkylsulfonil, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonil, halogen, cyano, nitro, or C3-C6 trialkylcylyl (R6 replaces hydrogen), C1-C6 alkyl, C2-C6 alkynil, C2-C6 alkynil, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinil, or (Chemical formula) R7, in each independent case, represents hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkylthio. M represents 0 to 4. X represents N, CH, CF, CCl, CBr, or CI. A represents –CH2OCH2-, -CH2S-, -CH2SCH2-, -CH2-N-(C1-C6 alkyl), -CH2N-(C1-C6 alkyl)CH2-, -CH[CO2(C1-C6 alkyl)]-, -CH(CN)-. -CH-(C1-C6 alkyl)-,-C(di-C1-C6 alkyl)- or –C=NO(C1-C6 alkyl)- Q represents a 5 or 6-membered heteroaromatic ring or an 8, 9 or 10-membered heterobicyclic ring system fused with an aromatic type, the ring system is not replaced, or is replaced once or more with identical or different substituents that can be selected. Free from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 al-kinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkyl sulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, or Q also represents a 5- or 6-membered heteroaromatic or heterocyclic ring system, or an 8, 9, or 10-membered aromatic fused heterocyclic ring system, where this ring or ring system is either unreplaced or replaced once or more by identical or different substituents that can be independently selected from hydrogen, C1-C6 alkyl, C2-C6 alkynyl. C2-C6 alkynil, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinil, C2-C6 haloalky-nil, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinil, C1-C4 alkylsulfonil, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinil, C1-C4 haloalkylsulfonil, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino. (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, or independently selectable substituents from phenyls or 5 or 6-membered heteroaromatic rings, which are possible for this phenyl or ring that is unsubstituted or substituted once or more, either the same or different from substituents of the types C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3- 15. Compounds of formula (I) according to claim 14 where R1 replaces hydrogen, amino, or hydroxyl, or replaces C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each of which is not substituted or is substituted once or more by identical or different substituents which can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, (C1-C4 alkoxy)carbonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, or (C1-C4 alkyl)C3-C6 cycloalkylamino. R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxycarbonyl, or C2-C6 alkylcarbonyl. R3 represents hydrogen, or represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl. Each of these may be independently selected to be replaced once or more times by identical or different substituent groups from the following categories: halogen, cyano, nitro, hydroxyl, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthione, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoxymino, C1-C4 alkylsulfoxymino-C1-C4 alkyl. C1-C4 alkyl sulfoxymino-C2-C5 alkyl carbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkyl carbonyl, or C3-C6 trialkyl silyl. R4 replaces hydrogen. Halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkyl thio, C1-C4 alkyl sulfonyl, C1-C4 alkyl sulfonyl, C1-C4 haloalkyl thio, C1-C4 haloalkyl sulfonyl, C1-C4 haloalkyl sulfonyl. Two C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl R4 atoms connected by an adjacent carbon atom may form a ring representing -(CH2)3-, -(CH2)4-,-(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)- or -(CH=CH-N=CH)-, with n representing 0 to 5. 3R5 represents C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C1-C6 halocycloalkyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, halogen, cyano, nitro, or C3-C6 trialkylcylyl. R6 represents hydrogen, C1-C6 alkyl. C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, or (chemical formula) R7, in each case independently, represents hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkylthio. m represents 0 to 4. X represents N, CH, CF, CCl, CBr, or CI. A represents -CH2C(CH3)2 or –C(CH3)2. Q represents a 5- or 6-membered heteroaromatic ring or a heterobisocyte ring system. A click that combines aromatic types with 8, 9, or 10 members, where this ring system is not replaced, or is replaced once or more with identical or different substituents that can be selected. Free from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 al-kinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkyl sulfenyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfenyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl) carbonyl, (C1-C6 alkoxy) carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino or N-oxide or salts of these substances. 16. Compounds of the formula (I-1) (I-1) (chemical formula) where R1 represents hydrogen, R2 represents hydrogen, R3 represents C1-C4 alkyl or cyano-C1-C3 alkyl, R4 represents hydrogen, methyl, trifluoromethyl, cyano, fluorine, chlorine, bromine, iodine. Or trifluoromethoxy. R5 represents methyl, fluorine, chlorine, bromine, or iodine. R7 represents fluorine, chlorine, or bromine. X represents N, CCl4, or CH3. A represents CH(CH3). Q represents the aromatic heterocyclic ring of the Q-37, Q-38, Q-39, Q-40, Q-58, and Q-59 series, which may be selected as a substituent at a single or multiple positions in the structure. It also represents the 5-member heterocyclic ring system Q-60, where these substituents can be independently selected from C1-C3 alkyl, C1-C3 haloalkyl, C1-C2 alkoxy, halogen, cyano, hydroxyl, nitro, or C1-C2 haloalkoxy. Or these substituents, which can be independently selected from phenyls or 5 or 6-membered heteroaromatic rings, are possible for phenyls or rings to be replaced at appropriate positions in the structure one or more times by different or similar substituents: C1-C6 alkyls, C2-C6 alkynyls, C2-C6 alkinyls, C3-C6 cycloalkyls, C1-C6 haloalkyls, C2-C6 haloalkinyls, C2-C6 haloalkinyls, C3-C6 halocycloalkyls, halogens, CN, NO2, C1-C4 alkoxy or C1-C4 haloalkoxy or N-oxides or salts of these substances. 17. Methods for controlling insect pests in animals which include the use of compounds. 18. Methods for controlling animal pests, which include the use of compounds of formulation (I) under claim 14 against animal pests and/or phytopathogenic fungi and/or their habitats and/or seeds. 19. Processes for the production of agricultural chemical components, which include the mixing of compounds of formulation (I) under claim 14 with additives and/or surface-active substances. 20. Methods for seed treatment, which include the use of compounds of formulation (I) under claim 14. 21. Methods for the treatment of genetically modified plants, which include the use of compounds of claim 14. 22. Methods for the treatment of seeds of genetically modified plants, which include the use of compounds under claim 14. 23. Seeds treated with compounds of formulation (I) under claim 14. 24. Methods for controlling animal pests, which include the use of compounds. Claim No. 15.25. Methods for controlling unwanted pests, which include the following: Compounds of formula (I) act on insect pests or their habitats, where the compound of formula (I) is (I) (chemical formula) where R1 replaces hydrogen, amino, or hydroxyl, or replaces C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each of which is either unsubstituted or substituted once or more by identical or different substituents which can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, (C1-C4 alkoxy) carbonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, or (C1-C4 alkyl)C3-C6 cycloalkylamino, R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxycarbonyl, or C2-C6 alkylcarbonyl. R3 represents hydrogen, or represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, C3-C12 cycloalkyl, C3-C12 cycloalkyl-C1-C6 alkyl, and C4-C12 bisocloalkyl, each of which may... Choose to replace one or more substitute groups with similar or different ones that can be selected. Obtained independently from halogens, cyano, nitro, hydroxyl, amino, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoximino, C1-C4 alkylsulfoximino-C1-C4 alkyl, C1-C4 alkylsulfoximino-C2-C5 alkylcarbonyl, C2-C6 alkoxycarbonyl. C2-C6 alkyl carbonyls, C3-C6 trialkylsilyls, or heteroaromatic rings with 5 or 6 members, R2 and R3 can be linked together through two to six carbon atoms, forming rings. A ring which is appropriately supplemented with nitrogen, sulfur, or oxygen atoms, and which, as appropriate, may be replaced one to four times with C1-C2 alkyl, halogen, cyano, amino, or C1-C2 alkoxy. R4 replaces hydrogen, halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkyl-thio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, C1-C4 haloalkylsulfonyl. Two C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl or R4, connected via adjacent carbon atoms, may form a ring representing -(CH2)3-, -(CH2)4-,-(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)-, or -(CH=CH-N=CH)- or R4. Two carbon atoms fuse together via adjacent carbon atoms, forming the following fused ring, which, as appropriate, is replaced by one or more identical or different substituents that can be independently selected from hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C3-C6 halocycloalkyl, halogen, C1-C6 alkoxy, C1-C4 alkylthio(C1-C6 alkyl), C1-C4 alkylsulfinyl(C1-C6 alkyl), C1-C4 alkylsulfonyl(C1-C6 alkyl), C1-C4 alkylamino, di(C1-C4 alkyl)amino, or C3-C6 cycloalkylamino (chemical formula). n represents 0 to 3, R5 represents C1-C6 alkyl. C3-C6 cycloalkyl, C1-C6 haloalkyl, C1-C6 halocycloalkyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkinyl, C2-C6 haloalkinyl, C1-C4 alkoxy, C1-C4 haloal-koxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, halogen, cyano, nitro, or C3-C6 trialkylsilyl (R6 replaces hydrogen), C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkinyl. C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, or (chemical formula) R7, in each case independently, represents hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkylthio. m represents 0 to 4. X represents N, CH, CF, CCl, CBr, or CI. A represents –CH2-, CH(CH)3C(CH3)2, or CH2CH2. Q represents a 5- or 6-membered heteroaromatic ring or an 8-, 9-membered, or heterobicyclic fused aromatic ring system. 10 members, the ring system is not replaceable, or replaced once or more with identical or different substitute groups that can be selected. Free from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 al-kinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkyl sulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, or Q also represents a 5- or 6-membered heteroaromatic or heterocyclic ring system, or an 8, 9, or 10-membered aromatic fused heterocyclic ring system, where this ring or ring system is either unreplaced or replaced once or more by identical or different substituents that can be independently selected from hydrogen, C1-C6 alkyl, C2-C6 alkynyl. C2-C6 alkynil, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinil, C2-C6 haloalky-nil, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinil, C1-C4 alkylsulfonil, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinil, C1-C4 haloalkylsulfonil, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino. (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, or independently selectable substituents from phenyls or 5 or 6-membered heteroaromatic rings, which are possible for this phenyl or ring that is unsubstituted or substituted once or more, either the same or different from substituents of the types C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3- C6 halocycloalkyl, halogen, CN, NO2, OH, C1-C4 alkoxy, C1-C4 haloalkoxy or salts of these substances. 26. Method according to claim 25 where R1 replaces hydrogen, amino or hydroxyl, or replaces C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each of which is not substituted or is substituted once or more by identical or different substituents which can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, (C1-C4 alkoxy)carbonyl, C1-C4 alkylamino, Di(C1-C4 alkyl)amino, C3-C6 cycloalkyl-amino, or (C1-C4 alkyl)C3-C6 cycloalkylamino. R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxy-carbonyl, or C2-C6 alkylcarbonyl. R3 represents hydrogen, or represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, each of which may be replaced once or... Furthermore, they are composed of similar or different substituent groups that can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthione, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoxymino, C1-C4 alkylsulfoxymino-C1-C4 alkyl, C1-C4 alkylsulfoxymino-C2-C5 alkylcarbonyl. C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, or C3-C6 trialkylsilyl, R4 replaces hydrogen, halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino. Two C3-C6 cycloalkylamino, (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl, or R4, connected via adjacent carbon atoms, may form a ring representing -(CH2)3-, -(CH2)4-,-(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)- or -(CH=CH-N=CH)-, n representing 0 to 3, and R5 representing C1-C6 alkyl, C3-C6 cycloalkyl. C1-C6 haloalkyl, C1-C6 halocycloalkyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, halogen, cyano, nitro, or C3-C6 trialkylcylyl (R6 replaces hydrogen), C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl. C1-C6 haloalkyl, C2-C6 haloalkinyl, or (chemical formula) R7, in each case independently, replace hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkylthio. m represents 0 to 4. X represents N, CH, CF, CCl, CBr, or CI. A represents -CH2-, CH(CH3)C(CH3)2, or CH2CH2. Q represents a 5- or 6-membered heteroaromatic ring, or an 8, 9, or 10-membered heterobicyclic ring system fused to an aromatic type, where this ring system is not replaced. Replaced once or more with identical or different substituents that can be selected by... Free from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 al-kinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkyl sulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl) carbonyl, (C1-C6 alkoxy) carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino or salts of these substances. 27. Method according to claim 25 where the compound belongs to the formula (I-1) (I-1) (chemical formula) where R1 represents hydrogen, R2 represents hydrogen, R3 represents C1-C4 alkyl, R4 represents hydrogen, methyl, trifluoromethyl, cyano, fluorine, chlorine, bromine, iodine or Trifluoromethoxy R5 represents methyl, fluorine, chlorine, bromine, or iodine; R7 represents fluorine, chlorine, or bromine; X represents N, CCl4, or CH4; A represents CH4 or CH(CH3); Q represents the aromatic heterocyclic ring of the Q-37, Q-38, Q-39, Q-40, Q-58, and Q-59 series, which may be selected as a substituent at a single or multiple positions in the structure; and also represents the 5-member heterocyclic ring system Q-60, where these substituents can be independently selected from C1-C3 alkyl, C1-C3 haloalkyl, C1-C2 alkoxy, halogen, cyano, hydroxyl, nitro, or C1-C2 haloalkoxy. Or these substituents, which can be independently selected from phenyls or 5- or 6-membered heteroaromatic rings, are possible for phenyls or rings to be substituted at appropriate positions in the structure one or more times by different or similar substituents: C1-C6 alkyls, C2-C6 alkynyls, C2-C6 alkinyls, C3-C6 cycloalkyls, C1-C6 haloalkyls, C2-C6 haloalkinyls, C2-C6 haloalkinyls, C3-C6 halocycloalkyls, halogens, CN, NO2, C1-C4 alkoxy or C1-C4 haloalkoxy or salts of these; Where the variable Q is defined as Q-37 (chemical formula), Q-38 (chemical formula), Q-39 (chemical formula), Q-40 (chemical formula), Q-58 (chemical formula), Q-59 (chemical formula), Q-60 (chemical formula) -----------------------------------------------

1. Compounds with structural formula (I) (chemical formula) (I), where R1 represents hydrogen, amino, or hydroxyl, or up to C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each of which is either unsubstituted or substituted one or more times in the structure by any identical or different substitutes that can be freely chosen from halogens, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkyl thio, C1-C4 alkyl sulfonyl, C1-C4 alkyl sulfonyl, (C1-C4 alkoxy)carbonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino. C3-C6 cycloalkylamino, or (C1-C4 alkyl)C3-C6 cycloalkylamino; R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkylamino, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxycarbonyl, or C2-C6 alkylcarbonyl; R3 represents hydrogen or represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, each of which is selectively replaced in the structure one or more times by a substitute substance. Identical or different structures that can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkyldetergent-simino, C1-C4 alkyldetergentsimino-C1-C4 alkyl, C1-C4 alkylsulfoxymino-C2-C5 alkylcarbonyl. C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, or C3-C6 trialkylsilyl, R3 also represents C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, each of which, by selection, is replaced one or more times in the structure with identical or different structural substituents that can be independently selected from amino, C3-C6 cycloalkylamino, or 5 or 6-membered heteroaromatic rings. R3 also represents C3-C12 cycloalkyl, C3-C12 cycloalkyl-C1-C6 alkyl, and C4-C12 bicycloalkyl, where the substituents in the structure can be independently selected from halogen, cyano, nitro, hydroxyl, amino, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylamino, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl. C1-C4 alkyl detergent simino, C1-C4 alkyl detergent simino-C1-C4 alkyl, C1-C4 alkyl detergent simino-C2-C5 alkyl carbonyl, C2-C6 alkoxy carbonyl, C2-C6 alkyl carbonyl, C3-C6 trialkyl silyl, or heteroaromatic rings with 5 or 6 members; R2 and R3 can fuse through 2 to 6 carbon atoms and form a ring which is further, as appropriate, has nitrogen, sulfur, or oxygen atoms added and, as appropriate, may be substituted 1 to 4 times in the structure by C1-C2 alkyl, halogen, cyano, amino, or C1-C2 alkoxy, R2 and R3 together also substitute. =S(C1-C4alkyl)4 or =S(O)(C1-C4alkyl)2; R4 represents hydrogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkylthio, C1-C4 alkylsulfenyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfenyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C4 alkoxy)amino. (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl, two R4 atoms passing through adjacent carbon atoms may form a ring representing -(CH2)3-, -(CH2)4-, -(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)-, -(CH=CH-N=CH)-, two R4 atoms passing through adjacent carbon atoms. Additionally, the following fused rings may form, which, depending on the circumstances, are substituted one or more times in the structure by the same or different structural substitutes. Which can be independently selected from hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C3-C6 halocycloalkyl, halogen, C1-C6 alkoxy, C1-C4 alkylthio(C1-C6 alkyl), C1-C4 alkylsulfinyl(C1-C6 alkyl), C1-C4 alkylsulfonyl(C1-C6 alkyl), C1-C4 alkylamino, di(C1-C4 alkyl)amino, or C3-C6 cycloalkylamino, (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (chemical formula) (Chemical formula) n represents 0 to 3, R5 represents C1-C6 alkyls, C3-C6 cycloalkyls, C1-C6 haloalkyls, C1-C6 halocycloalkyls, C2-C6 alkynyls, C2-C6 haloalkinyls, C2-C6 alkinyls, C2-C6 haloalkinyls, C1-C4 alkoxys, C1-C4 haloalkoxys, C1-C4 alkylthio, C1-C4 alkylsulfinyls, C1-C4 alkylsulfonyls, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyls, halogen, cyano, nitro, or C3-C6 trialkylsilyls, R6 represents hydrogen. C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl C2-C6 haloalkinyl, or (chemical formula) R6 also represents C3-C6 cycloalkyl, R7 in each case independently represents hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkylthio, m represents 0 to 4, X represents N, CH, CF, CCI, CBr, or CI, A represents -CH2-, -CH2O-, -CH2OCH2-, -CH2S-, -CH2SCH2-, -CN2N-(C1-C6 alkyl), -CH2N-(C1-C6 alkyl)CH2-. -CH[CO2(C1-C6 alkyl)]-, -CH(CN)-, -CH-(C1-C6 alkyl)-, -C(di-C1-C6 alkyl)-, -CH2CH2-, or -C=NO(C1-C6 alkyl)-, Q represents a 5- or 6-membered heteroaromatic ring or an 8, 9, or 10-membered aromatic fused heterobicyclic ring system, where the ring system is either unsubstituted or has one or more structural substitutions with identical or different substituents. Different compounds that can be selected independently include hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)imino. Q also represents heteroaromatic or heterocyclic ring systems with 5 or 6 members, or heterobicyclic ring systems fused to aromatic types with 8, 9, or 10 members, where the ring or ring system is either unsubstituted or has one or more substitutions in the structure by substituents. In identical or different structures that can be independently selected from hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)imino, or independently selectable substituents from phenyls or 5- or 6-membered heteroaromatic rings, where it is possible for this phenyl or ring to be unsubstituted or to be substituted one or more times with the same or different substituents. The structures include C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkinyl, C3-C6 cycloalkyl, C1-C6 halo-alkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogens, CN, NO2, OH, C1-C4 alkoxy, C1-C4 haloalkoxy, and also include N-oxides and salts.

2. Compounds with structural formula (I) according to claim 1, where R1 represents hydrogen, amino, or hydroxyl, or up to C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each of which is either unsubstituted or substituted one or more times by any identical or different structural substitutes which can be independently selected from halogen, cyano, nitro, hydroxyl, C1-C4 alkoxy, C1-C4 alkyl thio, C1-C4 alkyl sulfonyl, C1-C4 alkyl sulfonyl, (C1-C4 alkoxy)carbonyl, C1-C4 alkylamino, di(C1-C4 alkyl)amino. C3-C6 cycloalkylamino, or (C1-C4 alkyl)C3-C6 cycloalkylamino; R2 represents hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyyl, C1-C4 alkoxy, C1-C4 alkylamino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, C2-C6 alkoxycarbonyl, or C2-C6 alkylcarbonyl; R3 represents hydrogen or C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyyl, each of which is selectively replaced one or more times in the structure by an identical or different substitute that can be chosen independently. Continuing from halogen, cyano, nitro, hydroxyl, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylsulfimino, C1-C4 alkylsulfimino-C1-C4 alkyl, C1-C4 alkylsulfimino-C2-C5 alkylcarbonyl, C1-C4 alkylsulfoxymino, C1-C4 alkylsulfoxymino-C1-C4 alkyl, C1-C4 alkylsulfoxymino-C2-C5 alkylcarbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkyl carbonyl, or C3-C6 trialkyl silyl, R4 replaces hydrogen, halogen, cyano, nitro, C1-C4 alkyl, C1-C4 haloalkoxy, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkynyl, C1-C4 alkoxy, C1-C4 haloalkoxy, SF5, C1-C4 alkyl thio, C1-C4 alkyl sulfenyl, C1-C4 alkyl sulfonyl, C1-C4 haloalkyl thio, C1-C4 haloalkyl sulfenyl, C1-C4 haloalkyl sulfonyl, C1-C4 alkyl amino, di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino. (C1-C4 alkoxy)imino, (C1-C4 alkyl)(C1-C4 alkoxy)imino, (C1-C4 haloalkyl)(C1-C4 alkoxy)imino, or C3-C6 trialkylsilyl, two R4 atoms connected via adjacent carbon atoms. It may form a ring representing -(CH2)3-, -(CH2)4-, -(CH2)5-, -(CH=CH)2-, -OCH2O-, -O(CH2)2O-, -OCF2O-, -(CF2)2O-, -O(CF2)2O-, -(CH=CH- CH=N)-, -(CH=CH-N=CH)-, n representing 0 to 3, R5 representing C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C1-C6 halocycloalkyl, C2-C6 alkynyl, C2-C6 haloalkinyl, C2-C6 alkinyl, C2-C6 haloalkinyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfonyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfonyl, C1-C4 haloalkylsulfonyl, halogen, cyano, nitro, or C3-C6 trialkylsilyl, R6 replacing hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl C2-C6 haloalkyyl, or (chemical formula) R7, in each case independently, represents hydrogen, C1-C6 alkyl, C3-C6 cycloalkyyl, C1-C6 halo-alkyyl, halogen, cyano, nitro, C1-C4 alkoxy, C1-C4 haloalkyyl, C1-C4 alkylthio, C1-C4 alkylsulfinyl, or C1-C4 haloalkyylthio, m represents 0 to 4, X represents N, CH, CF, CCI, CBr, or CI, A represents -CH2-, -CH(CH3)C(CH3)2-, or -CH2CH2-, Q represents a 5 or 6-membered heteroaromatic ring or a heterobicyclic ring system. Aromatic fusions of 8, 9, or 10 members, where the ring system is either unreplaced or has had one or more structural substitutions with identical or different substituents. Different compounds that can be selected independently include hydrogen, C1-C6 alkyl, C2-C6 alkynyl, C2-C6 alkinyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkinyl, C2-C6 haloalkinyl, C3-C6 halocycloalkyl, halogen, CN, CO2H, CO2NH2, NO2, OH, C1-C4 alkoxy, C1-C4 halo-alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4 alkylamino. Di(C1-C4 alkyl)amino, C3-C6 cycloalkylamino, (C1-C6 alkyl)carbonyl, (C1-C6 alkoxy)carbonyl, (C1-C6 alkyl)aminocarbonyl, di(C1-C4 alkyl)aminocarbonyl, tri(C1-C2 alkyl)xylyl, and (C1-C4 alkyl)(C1-C4 alkoxy)amino, and also includes N-oxides and salts.

3. Compounds with the structural formula (I-1) (chemical formula) (I-1), where R1 represents hydrogen, R2 represents hydrogen, R3 represents hydrogen, C1-C4 alkyl (methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, or tert-butyl), or cyano-C1-C3 alkyl. (Cyanomethyl, 1-cyanoethyl, 2-cyano-ethyl, 1-cyano-n-propyl, 2-cyano-n-propyl, 3-cyano-n-propyl, 1-cyanoisopropyl, 2-cyanoisopropyl), R4 represents hydrogen, methyl, trifluoromethyl, cyano, fluorine, chlorine, bromine, iodine, or trifluoromethoxy, R5 represents methyl, fluorine, chlorine, bromine, or iodine, R6 represents fluorine, chlorine, or bromine, X represents N, CCI, or CH, A represents -CH2-, -CH(CH3)-, Q represents the aromatic heterocyclic ring of the Q-37, Q-38, Q-39, Q-40 series. Q-58 and Q-59, which are selectively substituted at one or more structural positions, and also include the 5-member heterocyclic ring system Q-60, where the substitutes in these structures can be independently selected from C1-C3 alkyl, C1-C3 haloalkyl, C1-C2 alkoxy, halogen, cyano, hydroxyl, nitro, or C1-C2 haloalkoxy, or independently selectable substitutes from phenyl or 5 or 6-member heteroaromatic rings. It is possible for phenyl or ring to be substituted at one or more suitable structural positions by the substitutes. These include different or similar terms such as C1-C6 alkyls, C2-C6 alkinyls, C2-C6 alkinils, C3-C6 cycloalkyls, C1-C6 haloalkyls, C2-C6 haloalkinyls, C2-C6 haloalkinils, C3-C6 halocycloalkyls, halogens, CN, NO2, C1-C4 alkoxy, or C1-C4 haloalkoxy, and also include N-oxides and their salts.

4. Derivatives of pyrazole carboxylic acid with structural formula (IV) (chemical formula) (IV), where A, Q, and R6 are defined as stated in claims 1 to 2.

5. Pyrazol carboxylic ester with structural formula (VI) (chemical formula) (VI), where A, Q, and R6 are defined as stated in claims 1 to 2, and R represents C1-C6 alkyl.

6. An alcohol with structural formula (X) (chemical formula) (X), where A and R6 are defined as stated in claims 1 to 2, and R represents C1-C6 alkyls.

7. The use of compounds with structural formula (I) as per claims 1 to 2 for the control of insect pests in animals.

8. Methods of controlling insect pests in animals, which are characterized by the compounds with structural formula (I) according to claims 1 to 2 being made active against insect pests in animals and/or phytopathogenic fungi and/or their habitats and/or seeds.

9. A process for the production of agrochemical components characterized by compounds with structural formula (I) according to claims 1 to 2 being mixed with extenders and/or surface active agents.

10. Use of compounds with structural formula (I) as per claims 1 to 2 for seed treatment.

11. Use of compounds with structural formula (I) as per claims 1 to 2 for gene-transplanted plants.

12. Use of compounds with structural formula (I) as per claims 1 to 2 for the treatment of seeds of gene-transplanted plants.