SU791199A3 - Акарицидное средство - Google Patents

Акарицидное средство Download PDF

Info

Publication number: SU791199A3
Authority: SU; USSR - Soviet Union
Prior art keywords: alkyl; substd; acaricidal; triazol; aryl
Prior art date: 1977-06-03

Application number

SU782623269A

Other languages

English (en)

Russian (ru)

Inventor

Хойбах Гюнтер

Эммель Людвиг

Вальтерсдорфер Анна

Original Assignee

Хехст Аг (Фирма)

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-06-03

Filing date

1978-06-02

Publication date

1980-12-23

1978-06-02 Application filed by Хехст Аг (Фирма) filed Critical Хехст Аг (Фирма)

1980-12-23 Application granted granted Critical

1980-12-23 Publication of SU791199A3 publication Critical patent/SU791199A3/ru

Links

150000001875 compounds Chemical class 0.000 claims abstract description 12
230000000895 acaricidal effect Effects 0.000 claims abstract description 10
239000013543 active substance Substances 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
239000000654 additive Substances 0.000 claims 1
230000000996 additive effect Effects 0.000 claims 1
239000000969 carrier Substances 0.000 claims 1
239000007788 liquid Substances 0.000 claims 1
239000000575 pesticide Substances 0.000 claims 1
235000017807 phytochemicals Nutrition 0.000 claims 1
229930000223 plant secondary metabolite Natural products 0.000 claims 1
239000007787 solid Substances 0.000 claims 1
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract description 5
125000000217 alkyl group Chemical group 0.000 abstract description 3
-1 methylenedioxy Chemical group 0.000 abstract description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 2
238000005904 alkaline hydrolysis reaction Methods 0.000 abstract 1
125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000004414 alkyl thio group Chemical group 0.000 abstract 1
150000004651 carbonic acid esters Chemical class 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
125000000753 cycloalkyl group Chemical group 0.000 abstract 1
125000004983 dialkoxyalkyl group Chemical group 0.000 abstract 1
125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 1
230000000855 fungicidal effect Effects 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
230000002363 herbicidal effect Effects 0.000 abstract 1
150000002431 hydrogen Chemical class 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
230000000749 insecticidal effect Effects 0.000 abstract 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
239000002904 solvent Substances 0.000 description 7
239000002253 acid Substances 0.000 description 5
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000000642 acaricide Substances 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
239000002585 base Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000376 reactant Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000001914 filtration Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
238000007363 ring formation reaction Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000007921 spray Substances 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000239290 Araneae Species 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
244000141359 Malus pumila Species 0.000 description 1
235000011430 Malus pumila Nutrition 0.000 description 1
235000015103 Malus silvestris Nutrition 0.000 description 1
241001454295 Tetranychidae Species 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001411 amidrazones Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000009835 boiling Methods 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
159000000011 group IA salts Chemical class 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
235000019252 potassium sulphite Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
230000009466 transformation Effects 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/72—Hydrazones
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)

SU782623269A 1977-06-03 1978-06-02 Акарицидное средство SU791199A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772725148 DE2725148A1 (de)	1977-06-03	1977-06-03	1-aryl-4-alkyl-1,2,4-triazol-5-one und verfahren zu ihrer herstellung

Publications (1)

Publication Number	Publication Date
SU791199A3 true SU791199A3 (ru)	1980-12-23

Family

ID=6010673

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU782623269A SU791199A3 (ru)	1977-06-03	1978-06-02	Акарицидное средство

Country Status (9)

Country	Link
EP (1)	EP0000014A1 (de)
JP (1)	JPS543071A (de)
BR (1)	BR7803552A (de)
DE (1)	DE2725148A1 (de)
ES (1)	ES470219A1 (de)
IL (1)	IL54831A0 (de)
IT (1)	IT1094947B (de)
SU (1)	SU791199A3 (de)
ZA (1)	ZA783182B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4318731A (en) *	1979-08-25	1982-03-09	Nihon Nohyaku Co., Ltd.	Δ2 -1,2,4-triazolin-5-one derivatives and herbicidal usage thereof
US4404019A (en) *	1980-12-24	1983-09-13	Sumitomo Chemical Company, Limited	3-Chloro-1-phenyl-1,2,4-triazolin-5-ones and their use as herbicides
CH651029A5 (de) *	1980-12-25	1985-08-30	Nihon Nohyaku Co Ltd	Triazolin-derivate, verfahren zu ihrer herstellung und sie enthaltende herbizide mittel.
US5084085A (en) *	1986-08-20	1992-01-28	Fmc Corporation	Herbicidal aryloxyphenyltriazolinones and related compounds
DE19521162A1 (de) *	1995-06-09	1996-12-12	Bayer Ag	N-Aryl-1,2,4-triazolin-5-one
AR052342A1 (es) *	2004-12-21	2007-03-14	Janssen Pharmaceutica Nv	Derivados sustituidos de triazolona,tetrazolona e imidazolona con actividad selectiva antagonista de alfa2c-adenoreceptores
US8546452B2 (en)	2005-10-12	2013-10-01	Toa Eiyo Ltd.	S1P3 receptor antagonist
CN105473558B (zh)	2013-06-20	2019-04-19	拜耳作物科学股份公司	作为杀螨剂和杀昆虫剂的芳基硫化物衍生物和芳基硫氧化物衍生物
BR112016000241B1 (pt)	2013-07-08	2021-06-22	Bayer Cropscience Aktiengesellschaft	Compostos pesticidas derivados de sulfeto de arila e sulfóxido de arila, formulação, seus usos, método para controle de pragas e método de proteção de semente ou planta
CN108024939B (zh)	2015-08-20	2024-06-07	联合利华知识产权控股有限公司	包封的内酰胺
KR20190110736A (ko)	2018-03-21	2019-10-01	주식회사유한양행	신규의 트라이아졸론 유도체 또는 이의 염 및 이를 포함하는 약학 조성물
KR20190110740A (ko)	2018-03-21	2019-10-01	주식회사유한양행	신규의 아릴 또는 헤테로아릴 트라이아졸론 유도체 또는 이의 염 및 이를 포함하는 약학 조성물
TW202039486A (zh)	2018-12-14	2020-11-01	南韓商柳韓洋行股份有限公司	三唑并吡啶-3-酮化物或其鹽及包含彼之醫藥組合物
TWI835945B (zh)	2018-12-14	2024-03-21	南韓商柳韓洋行股份有限公司	3,3-二氟烯丙胺化物或其鹽及包含彼的醫藥組合物

1977
- 1977-06-03 DE DE19772725148 patent/DE2725148A1/de active Pending
1978
- 1978-05-26 ES ES470219A patent/ES470219A1/es not_active Expired
- 1978-06-01 IL IL7854831A patent/IL54831A0/xx unknown
- 1978-06-01 EP EP78100026A patent/EP0000014A1/de not_active Withdrawn
- 1978-06-01 IT IT24121/78A patent/IT1094947B/it active
- 1978-06-02 SU SU782623269A patent/SU791199A3/ru active
- 1978-06-02 ZA ZA00783182A patent/ZA783182B/xx unknown
- 1978-06-02 BR BR787803552A patent/BR7803552A/pt unknown
- 1978-06-02 JP JP6587278A patent/JPS543071A/ja active Pending

Also Published As

Publication number	Publication date
IL54831A0 (en)	1978-08-31
IT7824121A0 (it)	1978-06-01
IT1094947B (it)	1985-08-10
JPS543071A (en)	1979-01-11
ES470219A1 (es)	1979-01-01
ZA783182B (en)	1979-06-27
DE2725148A1 (de)	1978-12-14
EP0000014A1 (de)	1978-12-20
BR7803552A (pt)	1979-02-20

Publication	Publication Date	Title
SU791199A3 (ru)	1980-12-23	Акарицидное средство
RU2015962C1 (ru)	1994-07-15	Производные валинамида в виде рацемата или в r(+)-конфигурации l-изомера, обладающие фунгицидной активностью
US3816419A (en)	1974-06-11	Substituted s-triazines
JPS6115062B2 (de)	1986-04-22
EP0104484A1 (de)	1984-04-04	Heterocyclische Verbindung und ihre Verwendung als Herbizid
CA1211108A (en)	1986-09-09	Heterocyclic phenyl ethers, processes for their preparation and herbicidal agents containing them
US5061731A (en)	1991-10-29	Novel n-benzyl-cyclopropanecarboxamide fungicides
US4082765A (en)	1978-04-04	Combating insects and mites with 1-carbamyl-4h-1,2,4-triazolin-5-ones and thiones
EP0286006B1 (de)	1992-05-20	Thiadiazol-Derivate und diese Derivate als wirksame Bestandteile enthaltende insektizide und mitizide Mittel
HU199059B (en)	1990-01-29	Fungicide compositions containina benzamide compounds as active components and process for producing the active components
JP2503547B2 (ja)	1996-06-05	カルバモイルトリアゾ―ル誘導体、その製造法およびそれを有効成分とする除草剤
KR880001318B1 (ko)	1988-07-23	벤조트리아졸의 제조방법
US3637729A (en)	1972-01-25	Perfluoroalkanesulfonamides n-substituted by heterocyclic groups
JPS63258462A (ja)	1988-10-25	２−フエノキシピリミジン誘導体及び除草剤
US4382954A (en)	1983-05-10	Fungicidal N-1-substituted cyclopropyl-N-acyl-2,6-dialkylaniline
JPH05202038A (ja)	1993-08-10	アゾール誘導体、その製造法およびそれを有効成分とする除草剤
JPS6231712B2 (de)	1987-07-09
JP2696252B2 (ja)	1998-01-14	シクロヘキサンカルボン酸誘導体並びにそれを含有する除草剤及び植物生長調節剤
US3933851A (en)	1976-01-20	Preparation of aromatic 2-imino-1,3-dithietanes
US3876796A (en)	1975-04-08	Anti-fungal composition and method
US3513237A (en)	1970-05-19	Pesticidal 2-trihalomethylbenzothiazoles
JP2530188B2 (ja)	1996-09-04	２−フェノキシピリミジン誘導体及び除草剤
US4174959A (en)	1979-11-20	Benzimidazole compounds
KR810000914B1 (ko)	1981-08-19	N,n'-메틸렌 비스-[0,0-디아릴 n-포스포노 메틸-글리시노 니트릴]의 제조방법
JPS62238258A (ja)	1987-10-19	ヒドラジンカルボキシレ−ト類およびこれを有効成分とする殺ダニ剤