SU719479A3 - Инсектицидное средство - Google Patents

Инсектицидное средство Download PDF

Info

Publication number: SU719479A3
Authority: SU; USSR - Soviet Union
Prior art keywords: hydrogen; methyl; chlorine; group; ethyl
Prior art date: 1972-02-04

Application number

SU731880508A

Other languages

English (en)

Russian (ru)

Inventor

Каррер Фридрих

Original Assignee

Циаб-Гейги 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.)

1972-02-04

Filing date

1973-01-31

Publication date

1980-02-29

1972-02-04 Priority claimed from CH169572A external-priority patent/CH568714A5/de

1972-02-16 Priority claimed from CH224072A external-priority patent/CH582473A5/de

1973-01-03 Priority claimed from CH4873A external-priority patent/CH584511A5/de

1973-01-31 Application filed by Циаб-Гейги Аг (Фирма) filed Critical Циаб-Гейги Аг (Фирма)

1980-02-29 Application granted granted Critical

1980-02-29 Publication of SU719479A3 publication Critical patent/SU719479A3/ru

Links

239000002917 insecticide Substances 0.000 title claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 32
239000001257 hydrogen Substances 0.000 claims abstract description 32
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 19
150000002431 hydrogen Chemical class 0.000 claims abstract description 14
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 9
229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
239000001301 oxygen Substances 0.000 claims abstract description 8
239000011203 carbon fibre reinforced carbon Substances 0.000 claims abstract description 4
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 4
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims abstract description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 3
229920002554 vinyl polymer Polymers 0.000 claims abstract description 3
125000000217 alkyl group Chemical group 0.000 claims abstract 3
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract 2
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims abstract 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 16
229910052801 chlorine Inorganic materials 0.000 claims description 16
239000000460 chlorine Substances 0.000 claims description 16
239000013543 active substance Substances 0.000 claims description 9
230000000749 insecticidal effect Effects 0.000 claims description 5
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
239000000654 additive Substances 0.000 claims 2
230000000996 additive effect Effects 0.000 claims 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
-1 chloro, methyl Chemical group 0.000 claims 1
230000002708 enhancing effect Effects 0.000 claims 1
239000000546 pharmaceutical excipient Substances 0.000 claims 1
239000007787 solid Substances 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 9
229910052736 halogen Inorganic materials 0.000 abstract description 8
150000002367 halogens Chemical class 0.000 abstract description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 2
125000003545 alkoxy group Chemical group 0.000 abstract 2
150000001721 carbon Chemical group 0.000 abstract 1
229910052799 carbon Inorganic materials 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
150000002170 ethers Chemical class 0.000 abstract 1
239000004009 herbicide Substances 0.000 abstract 1
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
239000000243 solution Substances 0.000 description 5
241000238631 Hexapoda Species 0.000 description 4
238000012360 testing method Methods 0.000 description 4
241001127120 Dysdercus fasciatus Species 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
230000000699 topical effect Effects 0.000 description 3
241000256118 Aedes aegypti Species 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
241001641895 Dermestes Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
241001425477 Dysdercus Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000254105 Tenebrio Species 0.000 description 2
238000005804 alkylation reaction Methods 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
239000004593 Epoxy Substances 0.000 description 1
241000382353 Pupa Species 0.000 description 1
208000003152 Yellow Fever Diseases 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000004891 communication Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000006735 epoxidation reaction Methods 0.000 description 1
239000008187 granular material Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
208000037909 invasive meningococcal disease Diseases 0.000 description 1
235000015110 jellies Nutrition 0.000 description 1
239000008274 jelly Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/16—Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/263—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings the aromatic rings being non-condensed

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)
Epoxy Compounds (AREA)

SU731880508A 1972-02-04 1973-01-31 Инсектицидное средство SU719479A3 (ru)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CH169572A CH568714A5 (en)	1972-02-04	1972-02-04	Pesticidal subst hydrocarbyl ethers - with effects on insects and acarina
CH224072A CH582473A5 (en)	1972-02-16	1972-02-16	Pesticidal subst hydrocarbyl ethers - with effects on insects and acarina
CH4873A CH584511A5 (en)	1973-01-03	1973-01-03	Pesticidal subst hydrocarbyl ethers - with effects on insects and acarina

Publications (1)

Publication Number	Publication Date
SU719479A3 true SU719479A3 (ru)	1980-02-29

Family

ID=27171733

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU731880508A SU719479A3 (ru)	1972-02-04	1973-01-31	Инсектицидное средство

Country Status (16)

Country	Link
JP (1)	JPS5844649B2 (2)
AT (1)	AT322279B (2)
BE (1)	BE794894A (2)
CA (1)	CA1045144A (2)
DD (1)	DD107383A5 (2)
DE (1)	DE2304962C2 (2)
EG (1)	EG10996A (2)
FI (1)	FI59389C (2)
FR (1)	FR2168115B1 (2)
GB (1)	GB1424211A (2)
HU (1)	HU165797B (2)
IL (1)	IL41419A (2)
IT (1)	IT986958B (2)
NL (1)	NL7301400A (2)
SE (2)	SE410184B (2)
SU (1)	SU719479A3 (2)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3998972A (en) *	1974-10-14	1976-12-21	Ciba-Geigy Corporation	Diphenyl derivatives
GB1570982A (en) *	1976-03-05	1980-07-09	Shell Int Research	Substituted benzyl ethers and thioethers
CH624087A5 (en) *	1976-08-25	1981-07-15	Hoechst Ag	Process for the preparation of phenoxyphenoxypropionic acid derivatives
FR2434133B1 (fr) *	1978-06-21	1988-04-29	Montedison Spa	Nouveaux diethers hydroquinoniques dotes d'une activite hormonale juvenile et acaricide
CH643223A5 (it) *	1978-06-21	1984-05-30	Montedison Spa	Dieteri idrochinonici aventi attivita ormonica giovanile e acaricida.
US4408076A (en) *	1981-06-05	1983-10-04	Zoecon Corporation	Phenoxy unsaturated carboxylic acid esters and derivatives
US4429167A (en)	1981-09-04	1984-01-31	Zoecon Corporation	3-Alkoxy-4-substituted-phenoxy-2,3-unsaturated acids, esters and derivatives
US4525205A (en) *	1982-01-22	1985-06-25	Zoecon Corporation	Herbicidal compositions comprising compounds containing a phenylaminophenoxy moiety
US4529438A (en) *	1982-03-23	1985-07-16	Zoecon Corp.	Pyridyloxy-phenoxy-alkanoic acid esters and derivatives
DK181683A (da) *	1983-04-25	1984-10-26	Cheminova As	Arylcycloalkylether-derivater, deres anvendelse og fremstilling
DE58907763D1 (de) *	1988-09-15	1994-07-07	Ciba Geigy	Neue Aether.
TW306864B (2) *	1993-10-19	1997-06-01	Sumitomo Chemical Co
US5398115A (en) *	1994-02-24	1995-03-14	Lin; Iyh-Han	Facsimile communication for locating and transmitting information from a document to selective call receivers
BR9506309A (pt) *	1994-08-04	1997-08-05	Sumitomo Chemical Co	Compostos de dihalopropeno agentes inseticidas/acaricidas contendo os mesmos e intermediários para a sua produção
TW307746B (2) *	1994-10-14	1997-06-11	Sumitomo Chemical Co
AU3856795A (en) *	1994-11-14	1996-06-06	Sumitomo Chemical Company, Limited	Dihalopropene compounds, use thereof, and intermediates for production thereof
DE69610204T2 (de) *	1995-04-18	2001-05-03	Sumitomo Chemical Co., Ltd.	Dihalopropen-verbindungen, diese enthaltende insektizide und intermediate zu ihrer herstellung
ATE182575T1 (de) *	1996-01-31	1999-08-15	Sumitomo Chemical Co	Fluorpropenverbindung, diese enthaltendes insektizid, und zwischenverbindung zu deren herstellung
JP4982950B2 (ja) *	2004-02-05	2012-07-25	住友化学株式会社	ピラゾール化合物とその製造中間体、ならびにその有害節足動物防除用途

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3155733A (en) *	1962-06-27	1964-11-03	Dow Chemical Co	Aryloxyarylthioalkenyl ethers
CH526258A (de) *	1970-03-25	1972-08-15	Hoffmann La Roche	Schädlingsbekämpfungsmittel
CH547060A (de) *	1970-04-17	1974-03-29	Hoffmann La Roche	Schaedlingsbekaempfungsmittel.

0
- BE BE794894D patent/BE794894A/xx unknown
1973
- 1973-01-23 FI FI173/73A patent/FI59389C/fi active
- 1973-01-25 SE SE7301031A patent/SE410184B/sv unknown
- 1973-01-29 IL IL41419A patent/IL41419A/xx unknown
- 1973-01-31 CA CA162,523A patent/CA1045144A/en not_active Expired
- 1973-01-31 NL NL7301400A patent/NL7301400A/xx not_active Application Discontinuation
- 1973-01-31 SU SU731880508A patent/SU719479A3/ru active
- 1973-02-01 DE DE2304962A patent/DE2304962C2/de not_active Expired
- 1973-02-02 FR FR7303688A patent/FR2168115B1/fr not_active Expired
- 1973-02-02 HU HUCI1335A patent/HU165797B/hu not_active IP Right Cessation
- 1973-02-02 DD DD168632A patent/DD107383A5/xx unknown
- 1973-02-02 AT AT94573A patent/AT322279B/de not_active IP Right Cessation
- 1973-02-02 IT IT19996/73A patent/IT986958B/it active
- 1973-02-02 GB GB538573A patent/GB1424211A/en not_active Expired
- 1973-02-03 JP JP48014204A patent/JPS5844649B2/ja not_active Expired
- 1973-02-03 EG EG43/73A patent/EG10996A/xx active
1978
- 1978-02-02 SE SE7801241A patent/SE7801241L/xx unknown

Also Published As

Publication number	Publication date
FI59389B (fi)	1981-04-30
DD107383A5 (2)	1974-08-05
DE2304962C2 (de)	1984-12-13
DE2304962A1 (de)	1973-08-09
JPS5844649B2 (ja)	1983-10-04
CA1045144A (en)	1978-12-26
IL41419A (en)	1978-08-31
EG10996A (en)	1976-09-30
JPS4886835A (2)	1973-11-15
IT986958B (it)	1975-01-30
NL7301400A (2)	1973-08-07
FR2168115A1 (2)	1973-08-24
SE410184B (sv)	1979-10-01
SE7801241L (sv)	1978-02-02
FR2168115B1 (2)	1978-04-21
IL41419A0 (en)	1973-03-30
GB1424211A (en)	1976-02-11
BE794894A (fr)	1973-08-02
AT322279B (de)	1975-05-12
HU165797B (2)	1974-11-28
FI59389C (fi)	1981-08-10

Publication	Publication Date	Title
SU719479A3 (ru)	1980-02-29	Инсектицидное средство
KR102282322B1 (ko)	2021-07-26	바퀴벌레 집합 유인 물질, 바퀴벌레 집합 유인제 및 바퀴벌레 구제제
SU671701A3 (ru)	1979-06-30	Инсектицидна композици
GB1078511A (en)	1967-08-09	Synthetic pyrethrin analogues and insecticidal compositions containing them
JPS5939808A (ja)	1984-03-05	衛生・農業害虫駆除剤
SU660566A3 (ru)	1979-04-30	Инсектицидна композици
Elliott et al.	1986	Insecticidal amides with selective potency against a resistant (super-kdr) strain of houseflies (Musca domestica L.)
HU196352B (en)	1988-11-28	Insecticide compositions containing substituted benzyl-ether derivatives as active ingredients and process for preparing the active substances
CN114375950A (zh)	2022-04-22	一种植物源美国白蛾天敌周氏啮小蜂引诱剂
US4334104A (en)	1982-06-08	Hydroquinone diether having juvenile hormone and acaricide activity
JPS6348203A (ja)	1988-02-29	害虫忌避剤
US4162326A (en)	1979-07-24	Insect control agents
JPH0352442B2 (2)	1991-08-12
AU621605B2 (en)	1992-03-19	Alkyl-aryl polyglycol ether interface agents for plant protection
CS219296B2 (en)	1983-03-25	Insecticide means and method of making the active substance
SU594884A3 (ru)	1978-02-25	Способ борьбы с насекомыми
EP0044718A2 (en)	1982-01-27	Pesticidal pentafluorobenzyl esters of cycloalkyl carboxylic acids
US3873724A (en)	1975-03-25	Method for disrupting normal insect maturation
GB2097393A (en)	1982-11-03	New antiparasitic and pesticidal derivatives of cyclopropane carboxylic acids
JPH0751525B2 (ja)	1995-06-05	ジフルオロハロメトキシフエニル誘導体およびそれを含有する殺虫、殺ダニ剤
US4412997A (en)	1983-11-01	Insect repellent compounds
FI76238B (fi)	1988-06-30	Insektattraheringsmedel, deras anvaendning och attraheringsfoerfarande.
US2349572A (en)	1944-05-23	Insecticide
US2795526A (en)	1957-06-11	Methods for repelling insects with polycyclic aldehydes and alcohols
SU609454A3 (ru)	1978-05-30	Средство дл борьбы с насекомыми