DD151868A5 - Insektizide und akarizide mittel - Google Patents

Insektizide und akarizide mittel Download PDF

Info

Publication number: DD151868A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; formula; substituted; insects; solvent
Prior art date: 1979-05-16

Application number

DD80221101A

Other languages

German (de)

English (en)

Inventor

Rainer Fuchs

Ingeborg Hammann

Bernhard Homeyer

Wolfgang Behrenz

Wilhelm Stendel

Original Assignee

Bayer Ag

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.)

1979-05-16

Filing date

1980-05-14

Publication date

1981-11-11

1980-05-14 Application filed by Bayer Ag filed Critical Bayer Ag

1981-11-11 Publication of DD151868A5 publication Critical patent/DD151868A5/de

Links

230000000895 acaricidal effect Effects 0.000 title claims abstract description 13
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230000000749 insecticidal effect Effects 0.000 claims abstract description 9
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WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
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RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
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239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
239000004540 pour-on Substances 0.000 description 1
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239000000047 product Substances 0.000 description 1
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239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000004544 spot-on Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
- C07D209/49—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide and having in the molecule an acyl radical containing a saturated three-membered ring, e.g. chrysanthemumic acid esters
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/17—Unsaturated ethers containing halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C62/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C62/30—Unsaturated compounds
- C07C62/34—Unsaturated compounds containing ether groups, groups, groups, or groups

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Furan Compounds (AREA)
Indole Compounds (AREA)

DD80221101A 1979-05-16 1980-05-14 Insektizide und akarizide mittel DD151868A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792919820 DE2919820A1 (de)	1979-05-16	1979-05-16	Fluor-substituierte oxyalkenyl-cyclopropancarbonsaeureester, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide und akarizide

Publications (1)

Publication Number	Publication Date
DD151868A5 true DD151868A5 (de)	1981-11-11

Family

ID=6070901

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD80221101A DD151868A5 (de)	1979-05-16	1980-05-14	Insektizide und akarizide mittel

Country Status (14)

Country	Link
US (1)	US4297366A (fr)
EP (1)	EP0020954A1 (fr)
JP (1)	JPS55162744A (fr)
AU (1)	AU5834080A (fr)
BR (1)	BR8003055A (fr)
DD (1)	DD151868A5 (fr)
DE (1)	DE2919820A1 (fr)
DK (1)	DK212680A (fr)
ES (1)	ES491522A0 (fr)
GR (1)	GR68493B (fr)
IL (1)	IL60064A (fr)
NZ (1)	NZ193697A (fr)
PL (1)	PL224224A1 (fr)
ZA (1)	ZA802878B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3140092A1 (de) *	1981-10-09	1983-04-21	Bayer Ag, 5090 Leverkusen	Substituierte vinylcyclopropancarbonsaeure-(6-phenoxy-2-pyridinyl)-methylester, verfahren zu ihrer herstellung sowie ihre verwendung als schaedlingsbekaempfungsmittel
DE3208334A1 (de) *	1982-03-09	1983-09-15	Bayer Ag, 5090 Leverkusen	Pestizide pour-on-formulierungen
AU615879B2 (en) *	1986-08-27	1991-10-17	Montedison S.P.A.	Derivatives of 2,2-dimethyl-cyclopropanecarboxylic acid
CN100500649C (zh) *	2007-08-03	2009-06-17	华东师范大学	偏卤菊酸α-氰基-4-氟-3-苯醚苄酯、其制备方法和所述化合物的用途

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1287080B (de)	1965-01-14	1969-01-16	Thomae Gmbh Dr K	Verfahren zur Herstellung von Alkoxyolefinen
FR2013334A1 (fr) *	1968-05-31	1970-04-03	Sumitomo Chemical Co
AU432259B1 (en)	1970-02-26	1972-08-24	Sumitomo Chemical Company, Limited	Novel substituted chrysanthemates
DE2326077C2 (de)	1972-05-25	1985-12-12	National Research Development Corp., London	Ungesättigte Cyclopropancarbonsäuren und deren Derivate, deren Herstellung und diese enthaltende Insektizide
FR2213013B1 (fr)	1972-11-10	1976-08-20	Roussel Uclaf
JPS5910336B2 (ja)	1975-08-01	1984-03-08	住友化学工業株式会社	第一菊酸エステルの不斉合成法
DE2650534A1 (de)	1976-11-04	1978-05-11	Bayer Ag	Verfahren zur herstellung von cyclopropancarbonsaeureestern
US4431668A (en)	1977-12-01	1984-02-14	Dainippon Jochugiku Kabushiki Kaisha	Cyclopropane carboxylic acid ester derivatives
BG48333A3 (en)	1978-02-28	1991-01-15	Montedison Spa	Method for preparing of 2, 2- dimethyl cyclopropane carbonic acid derivatives

1979
- 1979-05-16 DE DE19792919820 patent/DE2919820A1/de not_active Withdrawn
1980
- 1980-04-23 US US06/142,928 patent/US4297366A/en not_active Expired - Lifetime
- 1980-05-06 EP EP80102449A patent/EP0020954A1/fr not_active Withdrawn
- 1980-05-13 IL IL60064A patent/IL60064A/xx unknown
- 1980-05-13 NZ NZ193697A patent/NZ193697A/xx unknown
- 1980-05-13 AU AU58340/80A patent/AU5834080A/en not_active Abandoned
- 1980-05-14 DK DK212680A patent/DK212680A/da not_active Application Discontinuation
- 1980-05-14 JP JP6290380A patent/JPS55162744A/ja active Pending
- 1980-05-14 ZA ZA00802878A patent/ZA802878B/xx unknown
- 1980-05-14 ES ES491522A patent/ES491522A0/es active Granted
- 1980-05-14 PL PL22422480A patent/PL224224A1/xx unknown
- 1980-05-14 DD DD80221101A patent/DD151868A5/de unknown
- 1980-05-14 GR GR61941A patent/GR68493B/el unknown
- 1980-05-16 BR BR8003055A patent/BR8003055A/pt unknown

Also Published As

Publication number	Publication date
NZ193697A (en)	1982-05-25
ZA802878B (en)	1981-06-24
EP0020954A1 (fr)	1981-01-07
BR8003055A (pt)	1980-12-23
IL60064A (en)	1983-10-31
US4297366A (en)	1981-10-27
DK212680A (da)	1980-11-17
GR68493B (fr)	1982-01-07
DE2919820A1 (de)	1980-11-20
AU5834080A (en)	1980-11-20
JPS55162744A (en)	1980-12-18
PL224224A1 (fr)	1981-02-13
IL60064A0 (en)	1980-07-31
ES8107150A1 (es)	1980-12-16
ES491522A0 (es)	1980-12-16

Publication	Publication Date	Title
EP0019787B1 (fr)	1984-03-14	Esters d'acides 2-phénylalcén-1-yl-cyclopropane carboxyliques, procédé pour leur préparation et application comme insecticides et acaricides; intermédiaires pour leur préparation
EP0007576B1 (fr)	1983-11-16	Esters de dérivés du stilbène, procédé pour leur préparation, alcools de dérivés du stilbène comme produits intermédiaires, utilisation des esters comme insecticides
EP0001064B1 (fr)	1982-07-07	Derivés oxycarbonyles de phénoxybenzyles fluores; alcools phénoxybenzyliques fluorés et halogénures phénoxybenzyliques fluorés, procédés pour leur préparation et leur application
EP0004022B1 (fr)	1981-09-16	Dérivés pentafluorobenzyloxycarbonylés, méthode de préparation et leur utilisation comme insecticides et acaricides
EP0022970B1 (fr)	1983-06-01	Stéréoisomères d'esters alpha-cyano-3-phénoxy-4-fluor-benzyliques de l'acide 2,2-diméthyl-3-(2,2-dichloro-vinyl)-cyclopropane carboxylique, procédé pour leur préparation et leur application comme insecticides et acaricides
EP0121847B1 (fr)	1987-01-14	Esters d'acides 2,2-diméthyl-3-(2-halovinyl)-cyclopropanecarboxyliques, procédé pour leur préparation et leur utilisation comme pesticides
EP0043492B1 (fr)	1983-10-05	Esters d'acides 1-aryl-cyclopropan-1-carboxyliques, leur préparation et leur application comme insecticides
EP0033160B1 (fr)	1985-05-02	Esters substitués d'acide 3-(1,2-dibromo-alkyl)-2,2-diméthyl-cyclopropan-1-carboxylique, procédé et produits intermédiaires pour leur préparation et leur utilisation comme insecticides
EP0200943B1 (fr)	1988-12-07	Esters d'acides vinylcyclopropanecarboxyliques
EP0061053A1 (fr)	1982-09-29	4-Fluoro-3-phénoxy-benzylesters de l'acide 3-alcène-1-yl-2,2-diméthyl-cyclopropanecarboxylique, procédé pour leur préparation et leur utilisation en pesticides
EP0019090A1 (fr)	1980-11-26	Dérivés substitués de l'acide styrylcyclopropanecarboxylique, procédé pour leur préparation, leur utilisation, insecticides et acaricides, leur fabrication et procédé pour combattre les insectes
EP0029515B1 (fr)	1982-12-22	Benzylesters d'acide 2,2,3,3-tetraméthylpropanecarboxylique substitués par du fluor, procédé pour leur préparation et leur utilisation comme pesticides
EP0034731B1 (fr)	1985-10-30	Esters trifluorométhylbenzyliques, leurs intermédiaires, procédé pour leur préparation, et leur utilisation comme insecticides
EP0206167B1 (fr)	1989-01-04	Esters de l'acide tétraméthylcyclopropanecarbonique
EP0040742B1 (fr)	1983-07-13	Esters de l'acide 3-(chloro-3,3,4,4,4-pentafluoro-1-butényl)-2,2-diméthylcyclopropane carboxylique, procédé pour leur préparation et leur utilisation dans des insecticides
EP0026437B1 (fr)	1983-06-08	Esters fluorobenzyliques d'acide 3-(2,3-dichloro-3,3-difluoro-prop-1-én-1-yl)-2,2 diméthyl cyclopropane-carboxylique, procédé pour leur préparation et leur utilisation comme pesticides
EP0061114B1 (fr)	1984-12-12	Esters phénoxypyridylméthyl, procédé pour leur préparation et leur utilisation dans des compositions pesticides
EP0020954A1 (fr)	1981-01-07	Esters fluorés d'acides oxyalcénylcyclopropanecarboxyliques, procédé pour leur préparation, produits intermédiaires, leur préparation, insecticides et acaricides contenant les produits finals, leur préparation et leur utilisation
EP0076961A1 (fr)	1983-04-20	(6-Phénoxy-2-pyridinyl)méthyl esters d'acides vinylcyclopropane carboxyliques substitués, procédé pour leur préparation, et leur utilisation comme pesticides
DD147906A5 (de)	1981-04-29	Insektizide und akarizide mittel
EP0029543A1 (fr)	1981-06-03	Esters benzyliques fluorés d'acides spirocarboxyliques, procédé pour leur préparation et leur utilisation dans des pesticides
DE2939661A1 (de)	1981-04-23	Substituierte (alpha)-phenyl-carbonsaeure-(3-phenoxy-benzyl)-ester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0006456A1 (fr)	1980-01-09	Esters de l'acide spiropentane carboxylique, procédé pour leur préparation, compositions insecticides et acaricides, utilisation des esters de l'acide spiropentane carboxylique pour la lutte contre les insectes ou les araignées et procédé pour la préparation d'insecticides ou d'acaricides