CH577792A5 - 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 - Google Patents

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

Info

Publication number: CH577792A5
Authority: CH; Switzerland
Prior art keywords: formula; parts; plant; active substance; acetone
Prior art date: 1972-09-01

Application number

CH1292072A

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

1976-07-30

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

1972-09-01 Priority to CH1292072A priority Critical patent/CH577792A5/de

1973-08-14 Priority to IL42977A priority patent/IL42977A/en

1973-08-16 Priority to CA73178980A priority patent/CA1048502A/fr

1973-08-22 Priority to US390648A priority patent/US3925379A/en

1973-08-29 Priority to DE19732343526 priority patent/DE2343526A1/de

1973-08-29 Priority to NL7311885A priority patent/NL7311885A/xx

1973-08-30 Priority to EG342/73A priority patent/EG11411A/xx

1973-08-31 Priority to AT759373A priority patent/AT331075B/de

1973-08-31 Priority to ZA736010A priority patent/ZA736010B/xx

1973-08-31 Priority to GB4117273A priority patent/GB1436242A/en

1973-08-31 Priority to FR7331509A priority patent/FR2197880B1/fr

1973-08-31 Priority to BE135190A priority patent/BE804307A/fr

1973-08-31 Priority to JP48098127A priority patent/JPS49124234A/ja

1976-07-30 Publication of CH577792A5 publication Critical patent/CH577792A5/de

Links

239000000575 pesticide Substances 0.000 title claims description 4
150000001875 compounds Chemical class 0.000 claims description 30
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
241000196324 Embryophyta Species 0.000 claims description 16
239000013543 active substance Substances 0.000 claims description 15
239000003795 chemical substances by application Substances 0.000 claims description 14
230000000749 insecticidal effect Effects 0.000 claims description 11
235000013312 flour Nutrition 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 8
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
239000004033 plastic Substances 0.000 claims description 7
229920003023 plastic Polymers 0.000 claims description 7
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 6
229910052802 copper Inorganic materials 0.000 claims description 6
239000010949 copper Substances 0.000 claims description 6
230000001419 dependent effect Effects 0.000 claims description 6
238000001035 drying Methods 0.000 claims description 6
230000000694 effects Effects 0.000 claims description 6
150000002431 hydrogen Chemical group 0.000 claims description 6
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125000004093 cyano group Chemical group *C#N 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
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229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 3
GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 3
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ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 abstract description 4
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MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 abstract 2
NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 2
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239000012141 concentrate Substances 0.000 description 6
239000002270 dispersing agent Substances 0.000 description 6
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MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
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125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
150000008056 dicarboxyimides Chemical class 0.000 description 1
QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000010433 feldspar Substances 0.000 description 1
IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
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
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
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 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
LPBRCCDJNXKICP-UHFFFAOYSA-N molport-019-745-580 Chemical compound C1=CC(Cl)=CC=C1N1C(=O)N2C(C=C3)CC3N2C1=O LPBRCCDJNXKICP-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
239000003791 organic solvent mixture Substances 0.000 description 1
150000002903 organophosphorus compounds Chemical class 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
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 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
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 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
159000000000 sodium salts Chemical class 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
239000000725 suspension Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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

- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

CH1292072A 1972-09-01 1972-09-01 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 CH577792A5 (en)

Priority Applications (13)

Application Number	Priority Date	Filing Date	Title
CH1292072A CH577792A5 (en)	1972-09-01	1972-09-01	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
IL42977A IL42977A (en)	1972-09-01	1973-08-14	N-phenyl-2,3-diazabicyclo(2,2,1)-hept-5-ene-and(2,2,2)-oct-5-ene2,3-dicarboximides,their manufacture and their use in pest control
CA73178980A CA1048502A (fr)	1972-09-01	1973-08-16	Dicarboximides
US390648A US3925379A (en)	1972-09-01	1973-08-22	N-(substituted phenyl)-2,3-diazabicyclo{8 2.2.2{9 oct-5-ene and {8 2,2.1{9 hept-5-ene,2,3-dicarboximides
DE19732343526 DE2343526A1 (de)	1972-09-01	1973-08-29	Neue imide
NL7311885A NL7311885A (fr)	1972-09-01	1973-08-29
EG342/73A EG11411A (en)	1972-09-01	1973-08-30	New dicarboximides and their use in pest control
AT759373A AT331075B (de)	1972-09-01	1973-08-31	Insektizide mittel
ZA736010A ZA736010B (en)	1972-09-01	1973-08-31	New dicarboximides
GB4117273A GB1436242A (en)	1972-09-01	1973-08-31	Dicarboximides
FR7331509A FR2197880B1 (fr)	1972-09-01	1973-08-31
BE135190A BE804307A (fr)	1972-09-01	1973-08-31	Dicarboximides et produits pesticides qui en contiennent
JP48098127A JPS49124234A (fr)	1972-09-01	1973-08-31

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1292072A CH577792A5 (en)	1972-09-01	1972-09-01	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

Publications (1)

Publication Number	Publication Date
CH577792A5 true CH577792A5 (en)	1976-07-30

Family

ID=4387610

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1292072A CH577792A5 (en)	1972-09-01	1972-09-01	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

Country Status (4)

Country	Link
AT (1)	AT331075B (fr)
BE (1)	BE804307A (fr)
CH (1)	CH577792A5 (fr)
ZA (1)	ZA736010B (fr)

1972
- 1972-09-01 CH CH1292072A patent/CH577792A5/de not_active IP Right Cessation
1973
- 1973-08-31 AT AT759373A patent/AT331075B/de not_active IP Right Cessation
- 1973-08-31 ZA ZA736010A patent/ZA736010B/xx unknown
- 1973-08-31 BE BE135190A patent/BE804307A/fr unknown

Also Published As

Publication number	Publication date
ZA736010B (en)	1974-08-28
AT331075B (de)	1976-08-10
BE804307A (fr)	1974-02-28
ATA759373A (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
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
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
DE2343347A1 (de)	1974-03-14	Neue imide
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
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
DE2147589C3 (de)	1974-10-31	Neuer Phosphorsäureester, Verfahren zu seiner Herstellung sowie diesen enthaltende Schädlingsbekämpfungsmittel
DE2343526A1 (de)	1974-03-14	Neue imide
CH643563A5 (en)	1984-06-15	1,3-Diaza-2-phosphacyclohexane derivatives
DE2147588C3 (de)	1974-07-11	Phosphor-(on>säureester, Verfahren zu ihrer Herstellung und Schädlingsbekämpfungsmittel
CH581429A5 (en)	1976-11-15	Pesticidal subst. benzyl (thio)ethers - prepd. by reacting subst. benzyl halides or sulphonates with (thio)phenols
DE1542662C (de)	1972-12-07	Eckige Klammer auf 2-Methyl-chinolyl-(8) eckige Klammer zu -N-methylcarbaminsäureester, seine Salze und seine Verwendung
CH604522A5 (en)	1978-09-15	(4,5)-Benzospiro-(2,4)-heptane-(1)-carboxylate esters
CH576226A5 (en)	1976-06-15	Aralkyl phenyl ethers and thioethers - with acaricidal and insecticidal activity
DE2540129A1 (de)	1976-03-25	Schaedlingsbekaempfungsmittel
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
CH585515A5 (en)	1977-03-15	4-Subst-diphenyl ethers - with acaricidal and insecticidal activity
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
CH571305A5 (en)	1976-01-15	Phenyl-or benzyl-alkynyl ethers - prepd from phenol and alkinylhalides used as insecticides, nematocides
CH617569A5 (en)	1980-06-13	Pesticides containing, as active ingredient, a 3-N-phenyl-carbamoyl-4-hydroxy-1,2-(benzo)pyrone derivative.
CH580915A5 (en)	1976-10-29	Alkyl aralkenyl ketones prepn. - useful as pesticides
CH616563A5 (en)	1980-04-15	Pesticide containing a 5-phenylcarbamoylbarbituric acid as active ingredient
CH590612A5 (en)	1977-08-15	Pesticidal compsns. contg. organophosphorus amidines - useful for control of insect and acarid parasites on plants and animals
CH569417A5 (en)	1975-11-28	O-(Substd-propenyl) (thio) phosphates - insecticides and acaricides active against all growth stages