SU645516A3 - Инсектицидное средство - Google Patents

Инсектицидное средство

Info

Publication number: SU645516A3
Authority: SU; USSR - Soviet Union
Prior art keywords: methyl; hydrogen; soil; insecticidal activity; active substance
Prior art date: 1976-03-19

Application number

SU772459654A

Other languages

English (en)

Russian (ru)

Inventor

Маурер Фритц

Рибель Ганс-Иохем

Шредер Рольф

Гамманн Ингеборг

Хомайер Бернгард

Original Assignee

Байер 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.)

1976-03-19

Filing date

1977-03-16

Publication date

1979-01-30

1977-03-16 Application filed by Байер Аг (Фирма) filed Critical Байер Аг (Фирма)

1979-01-30 Application granted granted Critical

1979-01-30 Publication of SU645516A3 publication Critical patent/SU645516A3/ru

Links

239000002917 insecticide Substances 0.000 title claims description 3
150000001875 compounds Chemical class 0.000 claims description 4
239000007788 liquid Substances 0.000 claims description 4
239000007787 solid Substances 0.000 claims description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 2
229910052739 hydrogen Inorganic materials 0.000 claims 2
239000001257 hydrogen Substances 0.000 claims 2
150000002460 imidazoles Chemical class 0.000 claims 2
230000000749 insecticidal effect Effects 0.000 claims 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
239000000969 carrier Substances 0.000 claims 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 claims 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
239000013543 active substance Substances 0.000 description 15
238000002360 preparation method Methods 0.000 description 14
239000002689 soil Substances 0.000 description 12
-1 cyclohexane Chemical compound 0.000 description 7
241000238631 Hexapoda Species 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
241001124076 Aphididae Species 0.000 description 4
241000196324 Embryophyta Species 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
240000007124 Brassica oleracea Species 0.000 description 3
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 3
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 3
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000945 filler Substances 0.000 description 3
235000013312 flour Nutrition 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
235000019568 aromas Nutrition 0.000 description 2
230000004071 biological effect Effects 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
239000000975 dye Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000004575 stone Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
XGWMLNHWOLUXOY-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-2-methyl-5-nitroimidazole-4-carboxamide Chemical compound CC1=NC(C(N)=O)=C([N+]([O-])=O)N1C1=CC=C(Cl)C(Cl)=C1 XGWMLNHWOLUXOY-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241001425390 Aphis fabae Species 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
241000256593 Brachycaudus schwartzi Species 0.000 description 1
229910021532 Calcite Inorganic materials 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
238000010171 animal model Methods 0.000 description 1
239000002969 artificial stone Substances 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000003958 fumigation Methods 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
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 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000011785 micronutrient Substances 0.000 description 1
235000013369 micronutrients Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
239000005416 organic matter Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000012360 testing method Methods 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/70—One oxygen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/86—Oxygen and sulfur atoms, e.g. thiohydantoin

Landscapes

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

SU772459654A 1976-03-19 1977-03-16 Инсектицидное средство SU645516A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19762611770 DE2611770A1 (de)	1976-03-19	1976-03-19	N,n-dimethyl-0- eckige klammer auf imidazol(5)yl eckige klammer zu -carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide

Publications (1)

Publication Number	Publication Date
SU645516A3 true SU645516A3 (ru)	1979-01-30

Family

ID=5972972

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU772459654A SU645516A3 (ru)	1976-03-19	1977-03-16	Инсектицидное средство

Country Status (20)

Country	Link
JP (1)	JPS52113963A (de)
AT (1)	ATA187277A (de)
AU (1)	AU2319377A (de)
BE (1)	BE852637A (de)
BR (1)	BR7701651A (de)
CH (1)	CH625510A5 (de)
DD (1)	DD129996A5 (de)
DE (1)	DE2611770A1 (de)
DK (1)	DK120177A (de)
ES (1)	ES456925A1 (de)
FR (1)	FR2344542A1 (de)
GB (1)	GB1518474A (de)
IL (1)	IL51455A (de)
NL (1)	NL7702856A (de)
PL (1)	PL101704B1 (de)
PT (1)	PT66302B (de)
SE (1)	SE7703040L (de)
SU (1)	SU645516A3 (de)
TR (1)	TR19191A (de)
ZA (1)	ZA771646B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3136328A1 (de) *	1981-09-12	1983-03-24	Bayer Ag, 5090 Leverkusen	N,n-dimethyl-o-imidazol-4-yl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT482304A (de) *	1949-08-22

1976
- 1976-03-19 DE DE19762611770 patent/DE2611770A1/de not_active Withdrawn
1977
- 1977-02-15 IL IL51455A patent/IL51455A/xx unknown
- 1977-03-11 AU AU23193/77A patent/AU2319377A/en not_active Expired
- 1977-03-14 PT PT66302A patent/PT66302B/de unknown
- 1977-03-16 GB GB11114/77A patent/GB1518474A/en not_active Expired
- 1977-03-16 SU SU772459654A patent/SU645516A3/ru active
- 1977-03-16 NL NL7702856A patent/NL7702856A/xx not_active Application Discontinuation
- 1977-03-16 DD DD7700197884A patent/DD129996A5/de unknown
- 1977-03-16 TR TR19191A patent/TR19191A/xx unknown
- 1977-03-16 CH CH330077A patent/CH625510A5/de not_active IP Right Cessation
- 1977-03-17 ES ES456925A patent/ES456925A1/es not_active Expired
- 1977-03-17 SE SE7703040A patent/SE7703040L/xx unknown
- 1977-03-17 BR BR7701651A patent/BR7701651A/pt unknown
- 1977-03-18 ZA ZA00771646A patent/ZA771646B/xx unknown
- 1977-03-18 JP JP2940277A patent/JPS52113963A/ja active Pending
- 1977-03-18 BE BE175919A patent/BE852637A/xx unknown
- 1977-03-18 DK DK120177A patent/DK120177A/da unknown
- 1977-03-18 AT AT187277A patent/ATA187277A/de not_active Application Discontinuation
- 1977-03-18 PL PL1977196752A patent/PL101704B1/pl not_active IP Right Cessation
- 1977-03-18 FR FR7708237A patent/FR2344542A1/fr active Granted

Also Published As

Publication number	Publication date
DE2611770A1 (de)	1977-09-29
ZA771646B (en)	1978-02-22
DD129996A5 (de)	1978-03-01
ATA187277A (de)	1978-11-15
PT66302A (de)	1977-04-01
PT66302B (de)	1978-08-10
BE852637A (fr)	1977-09-19
IL51455A0 (en)	1977-04-29
ES456925A1 (es)	1978-01-16
NL7702856A (nl)	1977-09-21
JPS52113963A (en)	1977-09-24
DK120177A (da)	1977-09-20
AU2319377A (en)	1978-09-14
FR2344542B1 (de)	1981-02-13
FR2344542A1 (fr)	1977-10-14
TR19191A (tr)	1978-09-01
IL51455A (en)	1979-11-30
PL196752A1 (pl)	1978-01-02
GB1518474A (en)	1978-07-19
CH625510A5 (en)	1981-09-30
PL101704B1 (pl)	1979-01-31
BR7701651A (pt)	1978-01-03
SE7703040L (sv)	1977-09-20

Publication	Publication Date	Title
SU691063A3 (ru)	1979-10-05	Инсектоакарицидное средство
SU686596A3 (ru)	1979-09-15	Инсектицидна композици
KR100235246B1 (ko)	1999-12-15	살충제 페닐히드라진 유도체
KR890000482B1 (ko)	1989-03-18	N-페닐카르바메이트 함유 살균성 조성물
RU2109012C1 (ru)	1998-04-20	Новые производные пиррола
CZ124894A3 (en)	1995-07-12	Phenylhydrazine derivatives, a pesticidal agent containing such compounds and method of controlling undesired insects
SU691062A3 (ru)	1979-10-05	Инсектицидное средство
DE68908789T2 (de)	1994-04-14	Insectizide N'-substituierte-N-alkylcarbonyl-N'-acylhydrazine und N'-substituierte-N-acyl-N'-alkylcarbonyl hydrazine.
WO1992008351A1 (en)	1992-05-29	Method for the treatment of nematodes in soil using furfural
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