CH596757A5 - N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates) - Google Patents

N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates)

Info

Publication number: CH596757A5
Authority: CH; Switzerland
Prior art keywords: parts; sep; methyl; formula; active ingredient
Prior art date: 1974-07-11

Application number

CH960874A

Other languages

German (de)

English (en)

Inventor

Jozef Dr Drabek

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.)

1974-07-11

Filing date

1974-07-11

Publication date

1978-03-15

1974-07-11 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1974-07-11 Priority to CH960874A priority Critical patent/CH596757A5/de

1975-07-02 Priority to SU752149602A priority patent/SU586819A3/ru

1975-07-08 Priority to DE2530439A priority patent/DE2530439C2/de

1975-07-09 Priority to EG406/75A priority patent/EG11823A/xx

1975-07-09 Priority to FR7521572A priority patent/FR2277818A1/fr

1975-07-09 Priority to NLAANVRAGE7508197,A priority patent/NL181357C/xx

1975-07-09 Priority to US05/594,381 priority patent/US4004031A/en

1975-07-10 Priority to ZA00754421A priority patent/ZA754421B/xx

1975-07-10 Priority to CY1076A priority patent/CY1076A/xx

1975-07-10 Priority to TR18467A priority patent/TR18467A/xx

1975-07-10 Priority to BR7504396*A priority patent/BR7504396A/pt

1975-07-10 Priority to IT25262/75A priority patent/IT1043990B/it

1975-07-10 Priority to BE158162A priority patent/BE831212A/fr

1975-07-10 Priority to GB29080/75A priority patent/GB1486969A/en

1975-07-11 Priority to JP50085749A priority patent/JPS5138417A/ja

1977-09-02 Priority to DO1977002600A priority patent/DOP1977002600A/es

1978-03-15 Publication of CH596757A5 publication Critical patent/CH596757A5/de

1980-08-21 Priority to KE3075A priority patent/KE3075A/xx

1980-10-13 Priority to GT198065796A priority patent/GT198065796A/es

1981-12-30 Priority to MY174/81A priority patent/MY8100174A/xx

Links

150000001875 compounds Chemical class 0.000 claims description 21
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
-1 methylthioethylimino Chemical group 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 2
241000238631 Hexapoda Species 0.000 claims 2
230000001419 dependent effect Effects 0.000 claims 2
239000004599 antimicrobial Substances 0.000 claims 1
230000000749 insecticidal effect Effects 0.000 abstract description 6
230000001069 nematicidal effect Effects 0.000 abstract description 2
239000004480 active ingredient Substances 0.000 description 17
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
239000008187 granular material Substances 0.000 description 7
239000000203 mixture Substances 0.000 description 7
239000000126 substance Substances 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
241000196324 Embryophyta Species 0.000 description 4
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
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 4
239000002904 solvent Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
241000256244 Heliothis virescens Species 0.000 description 3
241000256250 Spodoptera littoralis Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
241000607479 Yersinia pestis Species 0.000 description 3
239000002585 base Substances 0.000 description 3
235000019993 champagne Nutrition 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
241000426497 Chilo suppressalis Species 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
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
239000000969 carrier Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000006378 damage Effects 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
238000009472 formulation Methods 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000002574 poison Substances 0.000 description 2
231100000614 poison Toxicity 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000012545 processing Methods 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 1
NQCGQLNRJWMDSE-UHFFFAOYSA-N C(C)=NN(C(OSC)=O)C Chemical compound C(C)=NN(C(OSC)=O)C NQCGQLNRJWMDSE-UHFFFAOYSA-N 0.000 description 1
241000257161 Calliphoridae Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical class NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
240000002024 Gossypium herbaceum Species 0.000 description 1
235000004341 Gossypium herbaceum Nutrition 0.000 description 1
241000736227 Lucilia sericata Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229920005551 calcium lignosulfonate Polymers 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
235000013877 carbamide Nutrition 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
238000002156 mixing Methods 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
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
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
150000002903 organophosphorus compounds Chemical class 0.000 description 1
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 1
239000006072 paste Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002002 slurry Substances 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
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007858 starting material Substances 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
150000003512 tertiary amines Chemical class 0.000 description 1
238000010998 test method Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000012749 thinning agent Substances 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000000080 wetting agent Substances 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
- 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

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)

CH960874A 1974-07-11 1974-07-11 N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates) CH596757A5 (en)

Priority Applications (19)

Application Number	Priority Date	Filing Date	Title
CH960874A CH596757A5 (en)	1974-07-11	1974-07-11	N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates)
SU752149602A SU586819A3 (ru)	1974-07-11	1975-07-02	Инсектицидное средство
DE2530439A DE2530439C2 (de)	1974-07-11	1975-07-08	Bis-[0-(1-Alkylthio-äthylimino)-N-methyl-carbaminsäure]-N,N'-sulfide, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Schädlingsbekämpfungsmittel
EG406/75A EG11823A (en)	1974-07-11	1975-07-09	Bis-50-lalkylthio-ethylimino)-n-methylcarbamic acisulphides n.n.bi(acid a-alkylthio-ethylamino)-n-methyl carbamic as herbicides d)n,n'-sulphides
FR7521572A FR2277818A1 (fr)	1974-07-11	1975-07-09	Nouveaux n, n'-sulfures d'acides bis-(o-1-alcoyl-thio-ethylimino)-n-methylcarbamiques, utiles comme agents de lutte contre les parasites
NLAANVRAGE7508197,A NL181357C (nl)	1974-07-11	1975-07-09	Werkwijze voor het bereiden van n-methylcarbamidezuurderivaten, alsmede werkwijze voor het bereiden van preparaten voor het bestrijden van schadelijke organismen, waarbij een aldus verkregen n-methylcarbamidezuurderivaat wordt toegepast.
US05/594,381 US4004031A (en)	1974-07-11	1975-07-09	Bis-(O-1-alkylthio-ethylimino)-N-methyl-carbamic acid)-N,N'-sulphide insecticides
TR18467A TR18467A (tr)	1974-07-11	1975-07-10	Pestsidler
CY1076A CY1076A (en)	1974-07-11	1975-07-10	Bis-(0-1-alkylthio-ethylimino)-n-methyl-carbamic acid)-nn'-sulphides
ZA00754421A ZA754421B (en)	1974-07-11	1975-07-10	Bis-<0-(1-alkylthio-ethylimino)-n-methyl-carbamic acid>-n,n'-sulphides
BR7504396*A BR7504396A (pt)	1974-07-11	1975-07-10	Processo para a preparacao de compostos organicos e composicoes praguicidas a base destes
IT25262/75A IT1043990B (it)	1974-07-11	1975-07-10	Prodotti disinfestanti
BE158162A BE831212A (fr)	1974-07-11	1975-07-10	Nouveaux n,n'-sulfures d'acides bis-(0-1-alcoyl-thio-ethylimino)-n-methylcarbamiques, utiles comme agents de lutte contre les parasites
GB29080/75A GB1486969A (en)	1974-07-11	1975-07-10	Bis-(0-1-alkylthio-ethylimino)-n-methyl-carbamic acid)-n,n'-sulphides
JP50085749A JPS5138417A (en)	1974-07-11	1975-07-11	Jugaiseibutsubojozai oyobi sonoseiho
DO1977002600A DOP1977002600A (es)	1974-07-11	1977-09-02	Nuevos n,'n- sulfuros de acidos bis-(0-1-alquil-tioetilimino) -n-metilcarbamicos, un procedimiento para prepararlos y su aplicacion en la lucha contra los parasitos
KE3075A KE3075A (en)	1974-07-11	1980-08-21	Bis-(o-1-alkylthio-ethylimino)-n-methyl-carbamic acid)-n,n'-sulphides
GT198065796A GT198065796A (es)	1974-07-11	1980-10-13	Nuevos sulfuros de acidos contra parasitos.
MY174/81A MY8100174A (en)	1974-07-11	1981-12-30	Bis-co-1-alkylthio-ethylimino)-n-methyl-carbamic acid)-n,n-sulphides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH960874A CH596757A5 (en)	1974-07-11	1974-07-11	N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates)

Publications (1)

Publication Number	Publication Date
CH596757A5 true CH596757A5 (en)	1978-03-15

Family

ID=4353757

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH960874A CH596757A5 (en)	1974-07-11	1974-07-11	N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates)

Country Status (6)

Country	Link
BE (1)	BE831212A (fr)
CH (1)	CH596757A5 (fr)
DO (1)	DOP1977002600A (fr)
GT (1)	GT198065796A (fr)
SU (1)	SU586819A3 (fr)
ZA (1)	ZA754421B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4382957A (en)	1975-12-01	1983-05-10	Union Carbide Corporation	Symmetrical insecticidal bis-carbamate compounds

1974
- 1974-07-11 CH CH960874A patent/CH596757A5/de not_active IP Right Cessation
1975
- 1975-07-02 SU SU752149602A patent/SU586819A3/ru active
- 1975-07-10 BE BE158162A patent/BE831212A/fr not_active IP Right Cessation
- 1975-07-10 ZA ZA00754421A patent/ZA754421B/xx unknown
1977
- 1977-09-02 DO DO1977002600A patent/DOP1977002600A/es unknown
1980
- 1980-10-13 GT GT198065796A patent/GT198065796A/es unknown

Also Published As

Publication number	Publication date
BE831212A (fr)	1976-01-12
GT198065796A (es)	1982-04-06
SU586819A3 (ru)	1977-12-30
DOP1977002600A (es)	1989-06-09
ZA754421B (en)	1976-06-30

Legal Events

Date	Code	Title	Description
1994-09-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2530439C2 (de)	1983-03-03	Bis-[0-(1-Alkylthio-äthylimino)-N-methyl-carbaminsäure]-N,N'-sulfide, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Schädlingsbekämpfungsmittel
EP0077759B1 (fr)	1987-12-09	Phénylurées
EP0023884B1 (fr)	1983-07-20	N-phényl-N'-benzoylurées, procédé pour leur préparation, compositions contenant ces dérivés et leur utilisation comme pesticides
EP0016729B1 (fr)	1984-07-25	N-(p-aminophényl)-N'-benzoylurées substituées, procédé pour leur préparation, compositions contenant ces dérivés et leur utilisation en tant que pesticides; dérivés substitués par un groupement alcényle de la p-amino-aniline
DE2741437A1 (de)	1978-03-23	Anilinderivate, verfahren zu ihrer herstellung und schaedlingsbekaempfungsmittel
EP0036390B1 (fr)	1983-10-26	Diphényléther-urées à propriétés herbicides
DE2812622C2 (de)	1986-10-30	(2,3-Dihydro-2,2-dimethyl-benzofuran-7-yl-oxy-N-methyl-carbamoyl)-(N'-alkyl-carbamoyl)-sulfide, Verfahren zu deren Herstellung und diese Verbindungen enthaltende insektizide Mittel
EP0038776B1 (fr)	1983-09-21	Phénylurées
EP0040179B1 (fr)	1984-08-29	Phénylbenzoylurées
EP0030922B1 (fr)	1984-07-04	Ethinyl-phénylurées, procédé pour leur préparation et leur utilisation comme herbicides
EP0014674B1 (fr)	1983-10-05	Urées N-phényl-N'-benzoyliques substituées, procédés pour leur préparation, agents contenant ces composés et leur utilisation pour combattre les organismes nuisibles; 4-(propényloxy)-anilines substituées
DE2643476A1 (de)	1977-04-07	Schaedlingsbekaempfungsmittel
EP0008565A1 (fr)	1980-03-05	Bis-(phénoxy-alcoyl-2 imidazoline)-1,1' sulfides, procédé pour leur préparation, compositions les contenant comme composants actifs et leur utilisation comme pesticides
CH596757A5 (en)	1978-03-15	N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates)
EP0118392B1 (fr)	1987-08-12	Composés de N-benzoylurée utilisés comme pesticides
EP0014675A2 (fr)	1980-08-20	Urées N-phényl-N'-benzoyliques substituées, procédés pour leur préparation, agents contenant ces composés et leur utilisation pour combattre les organismes nuisibles
EP0007066B1 (fr)	1981-06-03	4-Alkyl- et 4-allyl-thio-, sulfinyl- et sulfonyl-méthyl-2-amino-6-N,N'-diméthylcarbamoyloxy-pyrimidines, procédé pour leur préparation, compositions les contenant et leur utilisation comme insecticides
DE2902861A1 (de)	1979-08-02	Mikrobizide mittel
CH592411A5 (en)	1977-10-31	Phenoxymethyl- and phenylthiomethyl-pyridine derivs - with insecticidal, acaricidal and plant-growth regulating activity
DE2700876A1 (de)	1977-07-21	Schaedlingsbekaempfungsmittel
DE1955892C3 (de)	1980-05-22	Verwendung eines Benzylthiolcarbamates als Herbizid
EP0010515B1 (fr)	1984-10-17	Dérivés du sulfure de N.N'-(N-méthylcarbamoyl-(2,2-dimethyl-(2H,3H)-dihydrobenzofuran-7-yloxy)-(N'.N".N"-trialcoyle urée), procédé pour leur préparation, compositions contenant ces dérivés comme composants actifs et leur utilisation commme insecticides
DE2727614A1 (de)	1978-01-05	N,n'-bis-carbaminsaeure-sulfid-derivate, verfahren zu ihrer herstellung sowie schaedlingsbekaempfungsmittel
DE2700915A1 (de)	1977-07-21	Verfahren zur bekaempfung von insekten
DE3133009A1 (de)	1982-04-08	N-pyridinyl-n'-benzoylharnstoffe