CH602005A5 - (3)-Phenoxy-benzyl styryl-cyclopropane carboxylates - Google Patents

(3)-Phenoxy-benzyl styryl-cyclopropane carboxylates

Info

Publication number: CH602005A5
Authority: CH; Switzerland
Prior art keywords: sep; test; larvae; hydrogen; parts
Prior art date: 1976-02-17

Application number

CH191076A

Other languages

German (de)

English (en)

Inventor

Willy Meyer

Saleem Dr Farooq

Odd Dr Kristiansen

Jozef Dr Drabek

Laurenz Gsell

Original Assignee

Ciba Geigy 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.)

1976-02-17

Filing date

1976-02-17

Publication date

1978-07-14

1976-02-17 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1976-02-17 Priority to CH191076A priority Critical patent/CH602005A5/de

1977-02-08 Priority to NL7701321A priority patent/NL7701321A/xx

1977-02-14 Priority to DE19772706184 priority patent/DE2706184A1/de

1977-02-15 Priority to FR7704227A priority patent/FR2341554A1/fr

1977-02-16 Priority to IL51466A priority patent/IL51466A/xx

1977-02-16 Priority to IT20351/77A priority patent/IT1076892B/it

1977-02-16 Priority to BE174957A priority patent/BE851465A/fr

1977-02-16 Priority to AT103577A priority patent/AT347744B/de

1977-02-16 Priority to GB6501/77A priority patent/GB1570928A/en

1977-02-17 Priority to SU772452851A priority patent/SU644355A3/ru

1977-02-17 Priority to JP1663577A priority patent/JPS52100455A/ja

1977-04-27 Priority to OA56153A priority patent/OA05647A/fr

1978-07-14 Publication of CH602005A5 publication Critical patent/CH602005A5/de

Links

230000000895 acaricidal effect Effects 0.000 claims abstract description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 45
239000004480 active ingredient Substances 0.000 claims description 31
238000012360 testing method Methods 0.000 claims description 26
150000001875 compounds Chemical class 0.000 claims description 22
229910052739 hydrogen Inorganic materials 0.000 claims description 18
239000001257 hydrogen Substances 0.000 claims description 18
150000002431 hydrogen Chemical group 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
239000000460 chlorine Chemical group 0.000 claims description 9
239000008187 granular material Substances 0.000 claims description 9
239000000126 substance Substances 0.000 claims description 9
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims description 8
239000002689 soil Substances 0.000 claims description 8
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ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
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HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
230000000694 effects Effects 0.000 claims description 4
235000013601 eggs Nutrition 0.000 claims description 4
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical group 0.000 claims description 4
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235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 2
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FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 claims description 2
238000011156 evaluation Methods 0.000 claims description 2
239000011521 glass Substances 0.000 claims description 2
230000001069 nematicidal effect Effects 0.000 claims description 2
238000009331 sowing Methods 0.000 claims description 2
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239000002253 acid Substances 0.000 abstract description 4
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239000002917 insecticide Substances 0.000 abstract description 2
150000004820 halides Chemical class 0.000 abstract 1
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ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
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235000012211 aluminium silicate Nutrition 0.000 description 5
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239000004495 emulsifiable concentrate Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000008096 xylene Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000007792 addition Methods 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
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239000000377 silicon dioxide Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
230000009885 systemic effect Effects 0.000 description 3
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WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
229910014033 C-OH Inorganic materials 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
229910014570 C—OH Inorganic materials 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
WABPPBHOPMUJHV-UHFFFAOYSA-N Sesamex Chemical compound CCOCCOCCOC(C)OC1=CC=C2OCOC2=C1 WABPPBHOPMUJHV-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
241000256250 Spodoptera littoralis Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
239000000969 carrier Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
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125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
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FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
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125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
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UXPPDBVMSPAPCL-UHFFFAOYSA-N 1-prop-1-ynoxyprop-1-yne Chemical compound CC#COC#CC UXPPDBVMSPAPCL-UHFFFAOYSA-N 0.000 description 1
HRQBQVOUHQTQFJ-UHFFFAOYSA-N 2,2-dimethyl-3-(2-phenylethenyl)cyclopropane-1-carboxylic acid Chemical compound OC(=O)C1C(C)(C)C1C=CC1=CC=CC=C1 HRQBQVOUHQTQFJ-UHFFFAOYSA-N 0.000 description 1
QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
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BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
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241000256113 Culicidae Species 0.000 description 1
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 1
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
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PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
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150000001342 alkaline earth metals Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
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230000009286 beneficial effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
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150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
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239000003085 diluting agent Substances 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
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238000009472 formulation Methods 0.000 description 1
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150000008282 halocarbons Chemical class 0.000 description 1
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PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
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SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
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229910052757 nitrogen Inorganic materials 0.000 description 1
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
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150000003018 phosphorus compounds Chemical class 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
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239000004033 plastic Substances 0.000 description 1
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FHQKDLNFTINTBW-UHFFFAOYSA-N prop-1-ynyl carbamate Chemical compound CC#COC(N)=O FHQKDLNFTINTBW-UHFFFAOYSA-N 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
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229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
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239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
ZOKXUAHZSKEQSS-UHFFFAOYSA-N tribufos Chemical compound CCCCSP(=O)(SCCCC)SCCCC ZOKXUAHZSKEQSS-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
244000045561 useful plants Species 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CH191076A 1976-02-17 1976-02-17 (3)-Phenoxy-benzyl styryl-cyclopropane carboxylates CH602005A5 (en)

Priority Applications (12)

Application Number	Priority Date	Filing Date	Title
CH191076A CH602005A5 (en)	1976-02-17	1976-02-17	(3)-Phenoxy-benzyl styryl-cyclopropane carboxylates
NL7701321A NL7701321A (nl)	1976-02-17	1977-02-08	Werkwijze voor de bereiding van een ester.
DE19772706184 DE2706184A1 (de)	1976-02-17	1977-02-14	Cyclopropancarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung
FR7704227A FR2341554A1 (fr)	1976-02-17	1977-02-15	Nouveaux esters d'acides cyclopropanecarboxyliques, leur preparation et leur application a la lutte contre les parasites
IL51466A IL51466A (en)	1976-02-17	1977-02-16	2-methyl-3-(2-phenylvinyl)-cyclo-propanecarboxylic acid esters with 3-phenoxybenzyl alcohol derivatives, their prepation and acaricidal and insecticidal compositions containing them
IT20351/77A IT1076892B (it)	1976-02-17	1977-02-16	Esteri dell'acido ciclopropan-carbossilico,procedimento per la loro preparazione e loro impiego come disinfestanti
BE174957A BE851465A (fr)	1976-02-17	1977-02-16	Nouveaux esters d'acides cyclopropanecarboxyliques
AT103577A AT347744B (de)	1976-02-17	1977-02-16	Mittel zur bekaempfung von insekten und vertretern der ordnung akarina
GB6501/77A GB1570928A (en)	1976-02-17	1977-02-16	Pesticidal cyclopropane carboxylic acid esters
SU772452851A SU644355A3 (ru)	1976-02-17	1977-02-17	Инсектоакарицидное средство
JP1663577A JPS52100455A (en)	1976-02-17	1977-02-17	Cyclopropane carboxylate ester process for preparing same and harmful living controlling agent containing same
OA56153A OA05647A (fr)	1976-02-17	1977-04-27	Nouveaux esters d'acides cyclopropanecarboxyliques, leur préparation et leur application à la lutte contre les parasites.

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH191076A CH602005A5 (en)	1976-02-17	1976-02-17	(3)-Phenoxy-benzyl styryl-cyclopropane carboxylates

Publications (1)

Publication Number	Publication Date
CH602005A5 true CH602005A5 (en)	1978-07-14

Family

ID=4221455

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH191076A CH602005A5 (en)	1976-02-17	1976-02-17	(3)-Phenoxy-benzyl styryl-cyclopropane carboxylates

Country Status (4)

Country	Link
AT (1)	AT347744B (fr)
BE (1)	BE851465A (fr)
CH (1)	CH602005A5 (fr)
SU (1)	SU644355A3 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0009708A1 (fr) *	1978-09-29	1980-04-16	Bayer Ag	Esters m-phénoxybenzyliques d'acides bromostyrylcyclopropane carboxyliques (I), procédés pour leur préparation, produits intermédiaires obtenus ainsi que leur préparation, compositions contenant les esters (I), utilisation des esters (I) et procédé de préparation des compositions insecticides ou acaricides

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4183942A (en)	1976-08-27	1980-01-15	Fmc Corporation	Insecticidal (β-phenyl-β-substituted-vinyl)cyclopropanecarboxylates
ZA775160B (en)	1976-08-27	1978-07-26	Fmc Corp	Insecticidal styryl- and substituted-styrylcyclopropanecarboxylates
DE2730515A1 (de)	1977-07-06	1979-01-18	Bayer Ag	Substituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
US4200644A (en)	1978-01-26	1980-04-29	Fmc Corporation	Arylthiovinylcyclopropanecarboxylate insecticides
US4215069A (en)	1979-06-18	1980-07-29	Fmc Corporation	Arylthiovinylcyclopropanecarboxylate intermediates

1976
- 1976-02-17 CH CH191076A patent/CH602005A5/de not_active IP Right Cessation
1977
- 1977-02-16 AT AT103577A patent/AT347744B/de not_active IP Right Cessation
- 1977-02-16 BE BE174957A patent/BE851465A/fr not_active IP Right Cessation
- 1977-02-17 SU SU772452851A patent/SU644355A3/ru active

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0009708A1 (fr) *	1978-09-29	1980-04-16	Bayer Ag	Esters m-phénoxybenzyliques d'acides bromostyrylcyclopropane carboxyliques (I), procédés pour leur préparation, produits intermédiaires obtenus ainsi que leur préparation, compositions contenant les esters (I), utilisation des esters (I) et procédé de préparation des compositions insecticides ou acaricides

Also Published As

Publication number	Publication date
SU644355A3 (ru)	1979-01-25
ATA103577A (de)	1978-05-15
BE851465A (fr)	1977-08-16
AT347744B (de)	1979-01-10

Legal Events

Date	Code	Title	Description
1987-10-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0000508B1 (fr)	1981-09-02	Phénylacétates de 2-oxypyridyle, leur procédé de préparation et leur utilisation comme pesticide
DE2805226A1 (de)	1978-08-17	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
CH602005A5 (en)	1978-07-14	(3)-Phenoxy-benzyl styryl-cyclopropane carboxylates
DE2805193A1 (de)	1978-08-17	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
DE2805312A1 (de)	1978-08-17	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
EP0001824B1 (fr)	1980-12-10	Esters 3-phénoxy-alpha-vinylbenzyliques d'acides vinylcyclopropane carboxyliques, procédé pour leur préparation et leur utilisation comme pesticides
EP0001795B1 (fr)	1981-01-07	Esters phénoxy-alpha-vinylbenzyliques d'acides cyclopropane carboxyliques, procédé pour leur préparation et leur utilisation comme pesticides
EP0007421B1 (fr)	1981-04-29	Esters d'acide alpha-isopropane-phénylacétique, leur préparation et leur utilisation comme pesticides
DE2829329A1 (de)	1979-01-25	Cyclopropankarbonsaeureester und ihre salze mit anorganischen und organischen saeuren, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
DE2848495A1 (de)	1979-05-17	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
EP0010727B1 (fr)	1984-01-18	Vinylcyclopropanecarboxylates de 3-phénoxy-alpha-vinylbenzyle, procédé pour leur préparation et leur utilisation comme pesticides
EP0008332B1 (fr)	1981-11-04	Esters d'acide cyclopropane-carboxylique, leur préparation et leur utilisation comme pesticides
EP0006600B1 (fr)	1981-09-16	Esters d'acide tétrahalogèneéthyl cyclopropane carboxylique, procédé pour leur préparation et leur utilisation comme herbicides
DE2805274A1 (de)	1978-08-17	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
DE2843073A1 (de)	1979-04-19	Cyclopropankarbonsaeure-phenoxybenzylester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
EP0029002B1 (fr)	1983-03-23	Phénylacétates, procédé pour leur préparation, et leur utilisation comme pesticides
EP0008331B1 (fr)	1982-01-20	Esters d'acide cyclopropane-carboxylique, leur préparation et leur utilisation comme pesticides
EP0008334B1 (fr)	1981-10-14	Esters d'acide alpha-phényl-alpha-cyclopropane-acétique, leur préparation et leur utilisation comme pesticides
EP0031023B1 (fr)	1982-12-15	Esters d'acides cyclopropane carboxyliques, procédé pour leur préparation et leur utilisation
EP0028584B1 (fr)	1983-02-16	Sulfinylamides, procédé pour leur préparation et leur utilisation comme pesticides
DE2742065A1 (de)	1978-03-23	Cyclopropancarbonsaeure-3-phenoxy- benzylester, verfahren zu ihrer herstellung und ihre verwendung
DE2750844A1 (de)	1978-05-18	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
AT351868B (de)	1979-08-27	Insektizides oder akarizides mittel
DE2925315A1 (de)	1980-01-10	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
CH604516A5 (en)	1978-09-15	Pyrethroid type insecticides and acaricides

CH602005A5 - (3)-Phenoxy-benzyl styryl-cyclopropane carboxylates - Google Patents

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Priority Applications (12)

Applications Claiming Priority (1)

Publications (1)

Family

ID=4221455

Family Applications (1)

Country Status (4)

Cited By (1)

Families Citing this family (5)

Cited By (1)

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