ChemicalBook Product Catalog Chemical pesticides Pesticide Intermediates 2,6-Dichlorobenzaldoxime

2,6-Dichlorobenzaldoxime

2,6-Dichlorobenzaldoxime Basic information
Product Name:2,6-Dichlorobenzaldoxime
Synonyms:2,6-DICHLOROBENZALDOXIME;2,6-DICHLOROBENZALOXIME;TIMTEC-BB SBB008012;(NE)-N-[(2,6-dichlorophenyl)methylidene]hydroxylamine;2,6-dichloro-benzaldehydoxime;2,6-dichlorobenzyloxime;Benzaldehyde, 2,6-dichloro-, oxime;2,6-DICHLOROBENZALDOXIM
CAS:25185-95-9
MF:C7H5Cl2NO
MW:190.03
EINECS:246-720-0
Product Categories:Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
Mol File:25185-95-9.mol
2,6-Dichlorobenzaldoxime Structure
2,6-Dichlorobenzaldoxime Chemical Properties
Melting point 147 °C
Boiling point 280.4±30.0 °C(Predicted)
density 1.38±0.1 g/cm3(Predicted)
pka10.06±0.10(Predicted)
BRN 2046662
InChIKeyYBSXDWIAUZOFFV-ONNFQVAWSA-N
CAS DataBase Reference25185-95-9(CAS DataBase Reference)
NIST Chemistry Reference2,6-Dichlorobenzaldoxime(25185-95-9)
EPA Substance Registry SystemBenzaldehyde, 2,6-dichloro-, oxime (25185-95-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-26-36/37/39
TSCA Yes
HazardClass IRRITANT
HS Code 2913000090
MSDS Information
ProviderLanguage
ALFA English
2,6-Dichlorobenzaldoxime Usage And Synthesis
Chemical PropertiesThis product is colorless solid, mp149～150℃, insoluble in water.
Uses2,6-Dichlorobenzaldehyde oxime is an important intermediate in the synthesis process of benzoyl urea insecticides. In addition, it is also a pharmaceutical intermediate for the production of diclofenac sodium penicillin.
SynthesisThe preparation method uses 2,6-dichloro-dichlorobenzyl as a raw material for oximation to obtain 2,6-dichlorobenzaldehyde oxime.
2,6-Dichlorobenzaldoxime 3-CHLORO-N-([3-(2,6-DICHLOROPHENYL)-4,5-DIHYDRO-5-ISOXAZOLYL]METHYL)-5-(TRIFLUOROMETHYL)-2-PYRIDINAMINE 3-Phenoxybenzaldehyde 2,5-Dichlorobenzaldehyde 3,5-Dichlorobenzaldehyde 3-(2,6-DICHLOROPHENYL)-3A,9B-DIHYDRO-4H-CHROMENO[3,4-D]ISOXAZOL-4-ONE 3-(Trifluoromethyl)benzaldehyde (2,6-DICHLORO-4-METHYLPYRIDIN-3-YL)([(([(2,6-DICHLOROPHENYL)METHYLENE]AMINO)OXY)CARBONYL]AMINO)METHANONE 2,6-DICHLORO-N'-(([(2,6-DICHLOROPYRIDIN-4-YL)AMINO]CARBONYL)OXY)-N-METHYLBENZENECARBOXIMIDAMIDE 4-Dimethylaminobenzaldehyde N'-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-3-(2,6-DICHLOROPHENYL)-N'-METHYL-4,5-DIHYDRO-5-ISOXAZOLECARBOHYDRAZIDE ETHYL 2-([([(2,6-DICHLOROISONICOTINOYL)OXY]IMINO)(2,6-DICHLOROPHENYL)METHYL]AMINO)ACETATE O1-(2-CHLOROACETYL)-2,6-DICHLORO-1-BENZENECARBOHYDROXIMAMIDE 5-[[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL](METHYL)AMINO]-3-(2,6-DICHLOROPHENYL)-3AH-PYRROLO[3,4-D]ISOXAZOLE-4,6(5H,6AH)-DIONE ETHYL 2-(((2,6-DICHLOROPHENYL)[(([(2,6-DICHLORO-4-PYRIDYL)AMINO]CARBONYL)OXY)IMINO]METHYL)AMINO)ACETATE 2-Nitrobenzaldehyde ETHYL 2-([(2,6-DICHLOROPHENYL)(HYDROXYIMINO)METHYL]AMINO)ACETATE 2,5-DICHLORO-3-[(([(2,6-DICHLOROPHENYL)METHYLENE]AMINO)OXY)CARBONYL]PYRIDINE
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