IL28694A - Benzaldoxime derivatives - Google Patents

Benzaldoxime derivatives

Info

Publication number: IL28694A
Authority: IL; Israel
Prior art keywords: nitrobenzaldoxime; formula; derivatives; benzaldoxime; pesticidal composition
Prior art date: 1966-09-29

Application number

IL28694A

Other languages

English (en)

Original Assignee

Rhone Poulenc Sa

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.)

1966-09-29

Filing date

1967-09-28

Publication date

1971-03-24

1967-09-28 Application filed by Rhone Poulenc Sa filed Critical Rhone Poulenc Sa

1971-03-24 Publication of IL28694A publication Critical patent/IL28694A/en

Links

VTWKXBJHBHYJBI-SOFGYWHQSA-N (ne)-n-benzylidenehydroxylamine Chemical class O\N=C\C1=CC=CC=C1 VTWKXBJHBHYJBI-SOFGYWHQSA-N 0.000 title claims description 19
239000000203 mixture Substances 0.000 claims description 18
238000000034 method Methods 0.000 claims description 10
230000000361 pesticidal effect Effects 0.000 claims description 8
238000006243 chemical reaction Methods 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 4
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 4
-1 benzyl halide Chemical class 0.000 claims description 4
238000009835 boiling Methods 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 4
239000002270 dispersing agent Substances 0.000 claims description 4
239000003995 emulsifying agent Substances 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
238000009736 wetting Methods 0.000 claims description 4
239000000080 wetting agent Substances 0.000 claims description 4
SYNHCENRCUAUNM-UHFFFAOYSA-N Nitrogen mustard N-oxide hydrochloride Chemical compound Cl.ClCC[N+]([O-])(C)CCCl SYNHCENRCUAUNM-UHFFFAOYSA-N 0.000 claims description 3
150000002923 oximes Chemical class 0.000 claims description 3
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 2
241000534944 Thia Species 0.000 claims 1
239000004480 active ingredient Substances 0.000 claims 1
150000008040 ionic compounds Chemical class 0.000 claims 1
239000000243 solution Substances 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 6
239000007787 solid Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000000227 grinding Methods 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
LZIYAIRGDHSVED-UHFFFAOYSA-N 1-(bromomethyl)-3-chlorobenzene Chemical compound ClC1=CC=CC(CBr)=C1 LZIYAIRGDHSVED-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
230000026030 halogenation Effects 0.000 description 2
238000005658 halogenation reaction Methods 0.000 description 2
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 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
GQMMRLBWXCGBEV-VMPITWQZSA-N (ne)-n-[(3-nitrophenyl)methylidene]hydroxylamine Chemical compound O\N=C\C1=CC=CC([N+]([O-])=O)=C1 GQMMRLBWXCGBEV-VMPITWQZSA-N 0.000 description 1
MTQKMPGBALVEDL-ZPCKWCKBSA-N (z,12r)-12-hydroxy-2-sulfooctadec-9-enoic acid Chemical class CCCCCC[C@@H](O)C\C=C/CCCCCCC(C(O)=O)S(O)(=O)=O MTQKMPGBALVEDL-ZPCKWCKBSA-N 0.000 description 1
OSOUNOBYRMOXQQ-UHFFFAOYSA-N 1-chloro-3-methylbenzene Chemical compound CC1=CC=CC(Cl)=C1 OSOUNOBYRMOXQQ-UHFFFAOYSA-N 0.000 description 1
125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000488583 Panonychus ulmi Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000011149 active material Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
239000010775 animal oil Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000007799 cork Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
230000003151 ovacidal effect Effects 0.000 description 1
244000045947 parasite Species 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
RPDAUEIUDPHABB-UHFFFAOYSA-N potassium ethoxide Chemical compound [K+].CC[O-] RPDAUEIUDPHABB-UHFFFAOYSA-N 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000012216 screening Methods 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003613 toluenes Chemical class 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000008096 xylene Substances 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- A01N35/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (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)

IL28694A 1966-09-29 1967-09-28 Benzaldoxime derivatives IL28694A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR78184A FR1517774A (fr)	1966-09-29	1966-09-29	Emploi d'oximes comme pesticides

Publications (1)

Publication Number	Publication Date
IL28694A true IL28694A (en)	1971-03-24

Family

ID=8618126

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL28694A IL28694A (en)	1966-09-29	1967-09-28	Benzaldoxime derivatives

Country Status (12)

Country	Link
US (1)	US3845126A (de)
AT (1)	AT276857B (de)
BE (1)	BE704454A (de)
CH (1)	CH468784A (de)
DE (1)	DE1668610A1 (de)
DK (1)	DK120186B (de)
ES (1)	ES345560A1 (de)
FR (1)	FR1517774A (de)
GB (1)	GB1130685A (de)
IL (1)	IL28694A (de)
NL (1)	NL6712910A (de)
SE (1)	SE333368B (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4192893A (en) *	1975-03-20	1980-03-11	U.S. Philips Corporation	Anti-depressive compounds
US4216329A (en) *	1975-06-26	1980-08-05	Philip Morris Incorporated	Method of producing γ-amino alcohols
CH632130A5 (en) *	1977-03-02	1982-09-30	Ciba Geigy Ag	Compositions on the basis of oxime ethers, oxime esters or oxime carbamates which are suitable in agriculture for crop protection
US4079149A (en) *	1977-06-30	1978-03-14	Shell Oil Company	Benzyl oxime ethers
DE2926408A1 (de) *	1978-07-03	1980-01-17	Shell Int Research	Benzyloxim-aether-derivate
US4263227A (en) *	1979-05-14	1981-04-21	Ppg Industries, Inc.	5-(2-Chloro-4-trifluoromethyl)-, or (4-trifluoromethyl or 2,6-dichloro-4-trifluoromethylphenoxy)-2-nitro-substituted carbonyl oxime-O-alkyl ethers
US4375981A (en) *	1979-05-14	1983-03-08	Ppg Industries, Inc.	Method for controlling weed growth using herbicidally 5-(2-chloro-4-trifluoromethyl)-, or (4-trifluoromethyl or 2,6-dichloro-4-trifluoromethylphenoxy)-2-nitro-substituted carbonyl oxime-O-alkyl ethers
AU6159680A (en) *	1979-08-24	1981-04-09	Rhone-Poulenc, Inc.	Ketoximinoether insecticides
USRE30634E (en) *	1979-08-27	1981-06-02	Shell Oil Company	Benzyl oxime ethers
IL75858A (en) *	1984-07-31	1989-02-28	Commw Scient Ind Res Org	Substituted benzyl ethers of oximes,their production and their use as arthropodicides
US4647698A (en) *	1984-09-13	1987-03-03	Sandoz Ltd.	Novel compositions
DE4244390A1 (de) *	1992-12-29	1994-06-30	Basf Ag	Verfahren zur Herstellung von Oximino-Derivaten und neue Oximino-Derivate

1966
- 1966-09-29 FR FR78184A patent/FR1517774A/fr not_active Expired
1967
- 1967-09-21 NL NL6712910A patent/NL6712910A/xx unknown
- 1967-09-25 US US00670432A patent/US3845126A/en not_active Expired - Lifetime
- 1967-09-28 DK DK483267AA patent/DK120186B/da unknown
- 1967-09-28 BE BE704454D patent/BE704454A/xx unknown
- 1967-09-28 CH CH1356067A patent/CH468784A/fr unknown
- 1967-09-28 GB GB44284/67A patent/GB1130685A/en not_active Expired
- 1967-09-28 IL IL28694A patent/IL28694A/en unknown
- 1967-09-28 SE SE13359/67A patent/SE333368B/xx unknown
- 1967-09-29 DE DE19671668610 patent/DE1668610A1/de active Pending
- 1967-09-29 ES ES345560A patent/ES345560A1/es not_active Expired
- 1967-09-29 AT AT885767A patent/AT276857B/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
BE704454A (de)	1968-03-28
FR1517774A (fr)	1968-03-22
SE333368B (de)	1971-03-15
AT276857B (de)	1969-12-10
ES345560A1 (es)	1968-11-16
DK120186B (da)	1971-04-26
US3845126A (en)	1974-10-29
NL6712910A (de)	1968-04-01
GB1130685A (en)	1968-10-16
CH468784A (fr)	1969-02-28
DE1668610A1 (de)	1971-09-23

Publication	Publication Date	Title
IL28694A (en)	1971-03-24	Benzaldoxime derivatives
JPS61227577A (ja)	1986-10-09	ヨードプロパルギルエーテル類、それらの製造法およびそれらの使用
JPS58116455A (ja)	1983-07-11	シクロヘキサン−１，３−ジオン誘導体
IE42628B1 (en)	1980-09-10	Oxadizolinone derivatives and compositions containing them
JPS62298563A (ja)	1987-12-25	置換された３−アミノ−２−ベンゾイル−シクロヘキシ−２−エノン類
US2792296A (en)	1957-05-14	Phenylhydrazinopropionitriles, herbicidal method and composition embodying same
US2805257A (en)	1957-09-03	1-ethynyl-cyclohexylthiols
JPH0339501B2 (de)	1991-06-14
US2689262A (en)	1954-09-14	Diethanolamine salt of alpha, alpha-dichloropropionic acid
US2953490A (en)	1960-09-20	Propylamine fungicides
US2289590A (en)	1942-07-14	Mercurated aliphatic nitrile
US2862022A (en)	1958-11-25	Dinitroalkylphenyl methacrylates
US3702241A (en)	1972-11-07	Pesticide compositions containing dicarbadodecahydroundecaborates
US4062951A (en)	1977-12-13	Organophosphorus compounds, compositions containing them and their method of use
WO1991001978A1 (fr)	1991-02-21	Derives de triazine
US3897553A (en)	1975-07-29	Process for combatting pests using organotin compounds
US4383849A (en)	1983-05-17	2,3-Dihydro-4-pyrone derivatives, their preparation the herbicidal compositions in which they are present and their use for selectively destroying weeds in crops
US3544305A (en)	1970-12-01	Herbicidal n-formyl alpha-haloacetanilides
US3185723A (en)	1965-05-25	O-alkyl, s, 1-phenyl-2-alkoxycarbonylethyl alkylphosphonothioates
US2365056A (en)	1944-12-12	Insecticidal and fungicidal materials
US3766270A (en)	1973-10-16	Alkylaminooxanil oximes
JPS60152475A (ja)	1985-08-10	複素環式除草剤
AU758051B2 (en)	2003-03-13	Chloroacetamide mixtures with suppressed precipitation
US2841518A (en)	1958-07-01	Fungicidal compositions
US3496277A (en)	1970-02-17	Fungicidal methods and compositions employing pentahalocyclopentadienylamines