CH573205A5 - N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione - Google Patents

N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione

Info

Publication number: CH573205A5
Authority: CH; Switzerland
Prior art keywords: parts; formula; active ingredient; cycloheptatriene; dione
Prior art date: 1972-09-01

Application number

CH1292372A

Other languages

German (de)

English (en)

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.)

1972-09-01

Filing date

1972-09-01

Publication date

1976-03-15

1972-09-01 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1972-09-01 Priority to CH1292372A priority Critical patent/CH573205A5/de

1973-08-23 Priority to IL43060A priority patent/IL43060A/en

1973-08-23 Priority to CA179,535A priority patent/CA1048030A/fr

1973-08-28 Priority to DE19732343347 priority patent/DE2343347A1/de

1973-08-29 Priority to NL7311886A priority patent/NL7311886A/xx

1973-08-29 Priority to US392830A priority patent/US3912735A/en

1973-08-29 Priority to DD173156A priority patent/DD106941A5/xx

1973-08-31 Priority to ZA736009A priority patent/ZA736009B/xx

1973-08-31 Priority to AT759273A priority patent/AT331074B/de

1973-08-31 Priority to GB4117373A priority patent/GB1436243A/en

1973-08-31 Priority to FR7331510A priority patent/FR2197881B1/fr

1973-08-31 Priority to SU731959051A priority patent/SU605521A3/ru

1973-08-31 Priority to JP48098128A priority patent/JPS4966831A/ja

1973-09-03 Priority to BE135237A priority patent/BE804367A/fr

1976-03-15 Publication of CH573205A5 publication Critical patent/CH573205A5/de

Links

CHVJITGCYZJHLR-UHFFFAOYSA-N cyclohepta-1,3,5-triene Chemical compound C1C=CC=CC=C1 CHVJITGCYZJHLR-UHFFFAOYSA-N 0.000 title abstract description 3
UDATXMIGEVPXTR-UHFFFAOYSA-N 1,2,4-triazolidine-3,5-dione Chemical compound O=C1NNC(=O)N1 UDATXMIGEVPXTR-UHFFFAOYSA-N 0.000 title description 2
239000002917 insecticide Substances 0.000 title description 2
239000000575 pesticide Substances 0.000 title description 2
241000238631 Hexapoda Species 0.000 claims description 2
150000001875 compounds Chemical class 0.000 abstract description 19
229910052801 chlorine Inorganic materials 0.000 abstract description 4
YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 abstract description 4
239000007800 oxidant agent Substances 0.000 abstract description 4
NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 2
JEHCHYAKAXDFKV-UHFFFAOYSA-J lead tetraacetate Chemical compound CC(=O)O[Pb](OC(C)=O)(OC(C)=O)OC(C)=O JEHCHYAKAXDFKV-UHFFFAOYSA-J 0.000 abstract 1
239000004480 active ingredient Substances 0.000 description 38
239000000460 chlorine Substances 0.000 description 18
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
239000003795 chemical substances by application Substances 0.000 description 15
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
239000008187 granular material Substances 0.000 description 14
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
239000013543 active substance Substances 0.000 description 10
239000000243 solution Substances 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
239000002904 solvent Substances 0.000 description 9
239000005995 Aluminium silicate Substances 0.000 description 8
235000012211 aluminium silicate Nutrition 0.000 description 8
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 8
239000000126 substance Substances 0.000 description 8
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230000001419 dependent effect Effects 0.000 description 6
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125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 5
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
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150000002191 fatty alcohols Chemical class 0.000 description 4
238000002156 mixing Methods 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
239000000047 product Substances 0.000 description 4
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
239000004033 plastic Substances 0.000 description 3
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OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
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PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
241000256250 Spodoptera littoralis Species 0.000 description 2
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230000000895 acaricidal effect Effects 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
239000002518 antifoaming agent Substances 0.000 description 2
229960000892 attapulgite Drugs 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000012876 carrier material Substances 0.000 description 2
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229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
WFPZPJSADLPSON-UHFFFAOYSA-N dinitrogen tetraoxide Chemical compound [O-][N+](=O)[N+]([O-])=O WFPZPJSADLPSON-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
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235000013601 eggs Nutrition 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
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238000000227 grinding Methods 0.000 description 2
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WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
ACKFDYCQCBEDNU-UHFFFAOYSA-J lead(2+);tetraacetate Chemical compound [Pb+2].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O ACKFDYCQCBEDNU-UHFFFAOYSA-J 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
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PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
150000002790 naphthalenes Chemical class 0.000 description 2
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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QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
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229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
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229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
235000012245 magnesium oxide Nutrition 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
235000010446 mineral oil Nutrition 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
231100001184 nonphytotoxic Toxicity 0.000 description 1
239000003791 organic solvent mixture Substances 0.000 description 1
150000002903 organophosphorus compounds Chemical class 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000002245 particle Substances 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical class O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
239000000419 plant extract Substances 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
150000004291 polyenes Chemical class 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000006798 ring closing metathesis reaction Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 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
238000002336 sorption--desorption measurement Methods 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
IXZDIALLLMRYOU-UHFFFAOYSA-N tert-butyl hypochlorite Chemical compound CC(C)(C)OCl IXZDIALLLMRYOU-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000002023 wood Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/18—Bridged systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH1292372A 1972-09-01 1972-09-01 N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione CH573205A5 (en)

Priority Applications (14)

Application Number	Priority Date	Filing Date	Title
CH1292372A CH573205A5 (en)	1972-09-01	1972-09-01	N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione
IL43060A IL43060A (en)	1972-09-01	1973-08-23	2-phenyl-5alpha,6,6alpha,7-tetrahydro-5,7-etheno-1h,5h-cyclopropa(d)(1,2,4)triazolo(1,2-alpha)pyridazine-1,3(2h)-diones,their manufacture and pesticidal compositions containing them
CA179,535A CA1048030A (fr)	1972-09-01	1973-08-23	Imides
DE19732343347 DE2343347A1 (de)	1972-09-01	1973-08-28	Neue imide
NL7311886A NL7311886A (fr)	1972-09-01	1973-08-29
US392830A US3912735A (en)	1972-09-01	1973-08-29	Dicarboximide derivatives
DD173156A DD106941A5 (fr)	1972-09-01	1973-08-29
ZA736009A ZA736009B (en)	1972-09-01	1973-08-31	New imides
AT759273A AT331074B (de)	1972-09-01	1973-08-31	Insektizides mittel
GB4117373A GB1436243A (en)	1972-09-01	1973-08-31	Imides
FR7331510A FR2197881B1 (fr)	1972-09-01	1973-08-31
SU731959051A SU605521A3 (ru)	1972-09-01	1973-08-31	Инсектицидное средство
JP48098128A JPS4966831A (fr)	1972-09-01	1973-08-31
BE135237A BE804367A (fr)	1972-09-01	1973-09-03	Carboximides et produits pesticides qui en contiennent

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1292372A CH573205A5 (en)	1972-09-01	1972-09-01	N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione

Publications (1)

Publication Number	Publication Date
CH573205A5 true CH573205A5 (en)	1976-03-15

Family

ID=4387644

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1292372A CH573205A5 (en)	1972-09-01	1972-09-01	N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione

Country Status (5)

Country	Link
AT (1)	AT331074B (fr)
BE (1)	BE804367A (fr)
CH (1)	CH573205A5 (fr)
SU (1)	SU605521A3 (fr)
ZA (1)	ZA736009B (fr)

1972
- 1972-09-01 CH CH1292372A patent/CH573205A5/de not_active IP Right Cessation
1973
- 1973-08-31 ZA ZA736009A patent/ZA736009B/xx unknown
- 1973-08-31 AT AT759273A patent/AT331074B/de active
- 1973-08-31 SU SU731959051A patent/SU605521A3/ru active
- 1973-09-03 BE BE135237A patent/BE804367A/fr unknown

Also Published As

Publication number	Publication date
BE804367A (fr)	1974-03-04
ZA736009B (en)	1974-08-28
AT331074B (de)	1976-08-10
SU605521A3 (ru)	1978-04-30
ATA759273A (de)	1975-10-15

Legal Events

Date	Code	Title	Description
1981-05-29	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0001203A1 (fr)	1979-04-04	N-phényl-N'-benzoyl-urées, procédé pour leur préparation, produits les contenant, et leur utilisation comme pesticides
DE2259960C2 (de)	1983-03-03	1.2.4-Triazolyl-(thiono)-phosphor(phosphon)-säureester, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
EP0004030A2 (fr)	1979-09-19	N-phényl-N'-fluorobenzoyl urées substituées, leurs procédés de préparation et leur utilisation comme pesticides
CH574214A5 (fr)	1976-04-15
CA1048030A (fr)	1979-02-06	Imides
CH573205A5 (en)	1976-03-15	N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione
DE2330089C2 (de)	1983-03-24	1.2.4-Triazolyl-(thiono)-phosphor(phosphon)-säurederivate, Verfahren zu ihrer Herstellung sowie diese enthaltende Schädlingsbekämpfungsmittel
DE2643428A1 (de)	1977-04-07	Schaedlingsbekaempfungsmittel
CH577792A5 (en)	1976-07-30	Substd-2,3-dicarboxamide pesticides - N-(substd phenyl)-2,3-diaza bicyclo-(2,2,1)-hept-5-ene-and -(2,2,2)-oct-5-enes
DE1642214A1 (de)	1971-04-22	Mittel und Verfahren zur Bekaempfung von Insekten,Spinnentieren und deren Entwicklungsstadien
AT318302B (de)	1974-10-10	Insektizide und akarizide Mittel
CH576226A5 (en)	1976-06-15	Aralkyl phenyl ethers and thioethers - with acaricidal and insecticidal activity
CH581429A5 (en)	1976-11-15	Pesticidal subst. benzyl (thio)ethers - prepd. by reacting subst. benzyl halides or sulphonates with (thio)phenols
DE2147589C3 (de)	1974-10-31	Neuer Phosphorsäureester, Verfahren zu seiner Herstellung sowie diesen enthaltende Schädlingsbekämpfungsmittel
CH604522A5 (en)	1978-09-15	(4,5)-Benzospiro-(2,4)-heptane-(1)-carboxylate esters
CH591809A5 (en)	1977-09-30	N-phenyl polycyclic imides - useful as pesticides, esp insecticides prepd from cycloheptatriene and a 1,2,4-triazolidin-3,5-dione
CH590612A5 (en)	1977-08-15	Pesticidal compsns. contg. organophosphorus amidines - useful for control of insect and acarid parasites on plants and animals
CH580915A5 (en)	1976-10-29	Alkyl aralkenyl ketones prepn. - useful as pesticides
CH571810A5 (en)	1976-01-30	N,N-dimethyl-N'-subst. formamidines - prepd. by reacting subst. S-methyl formamidinates with dimethylformamide dialkyl acetals
CH569417A5 (en)	1975-11-28	O-(Substd-propenyl) (thio) phosphates - insecticides and acaricides active against all growth stages
CH571304A5 (en)	1976-01-15	Subst. formamidine derivs prepn - with biocidal activity
CH590610A5 (en)	1977-08-15	Substd-2,3-dicarboxamide pesticides - N-(substd phenyl)-2,3-diaza bicyclo-(2,2,1)-hept-5-ene-and -(2,2,2)-oct-5-enes
CH563120A5 (en)	1975-06-30	Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides
CH563119A5 (en)	1975-06-30	S-benzyl dithiophosphoric esters - insecticides and acaricides
CH582993A5 (en)	1976-12-31	S'-(midomethylene)s-alkyl s-alkyldithiophosphoric esters - - insecticides, acaricides, nematocides and fungicides