4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride

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4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride Basic information
Product Name:4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride
Synonyms:4-[(AMINOOXY)METHYL]-1,2-DICHLOROBENZENE HYDROCHLORIDE;O-(3,4-Dichlorobenzyl)hydroxylamine hydrochloride;(3,4-dichlorophenyl)methoxyazanium,chloride;O-(3,4-dichlor-benzyl)-hydroxylamin hydrochloride;Benzyloxyamine, 3,4-dichloro-, hydrochloride;O-[(3,4-Dichlorophenyl)methyl]hydroxylamine hydrochloride;4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride
CAS:15256-10-7
MF:C7H8Cl3NO
MW:228.5
EINECS:
Product Categories:
Mol File:15256-10-7.mol
4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride Structure
4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride Chemical Properties
Melting point 195°
Boiling point 195°C
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly, Heated)
form Solid
color White to Off-White
Safety Information
Hazard Codes Xn
Risk Statements 22
HazardClass IRRITANT
HS Code 2928009090
MSDS Information
4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride Usage And Synthesis
Uses4-[(Aminooxy)methyl]-1,2-dichlorobenzenehydrochloride, has shown to act as inhibitor of indoleamine 2,3-dioxygenase-1. ndoleamine 2,3-dioxygenase-1 (IDO1) is a promising therapeutic target for the treatment of cancer, chronic viral infections, and other diseases characterized by pathol.
4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride Preparation Products And Raw materials
Tag:4-[(Ammoniooxy)methyl]-1,2-dichlorobenzene chloride(15256-10-7) Related Product Information
CITCO 2-[(Ammoniooxy)methyl]-1,4-dichlorobenzene chloride 1-[(Ammoniooxy)methyl]-2,3-dichlorobenzene chloride 6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime 4-[(4-Chlorophenyl)sulfanyl]-3-nitrobenzenecarbaldehyde O-(3,4-dichlorobenzyl)oxime 4-(6-Chloro-1-[(3,4-dichlorobenzyl)oxy]-1H-1,3-benzimidazol-2-yl)phenyl methyl ether 4-Chlorophenyl 3-([(3,4-dichlorobenzyl)oxy]imino)propanoate 1-(2,6-Dichlorobenzyl)-1H-indole-2,3-dione 3-[O-(3,4-dichlorobenzyl)oxime] N-[(3,4-Dichlorobenzyl)oxy]-N-(([(2,4-dichlorobenzyl)oxy]imino)methyl)urea 2-(2-Chlorophenyl)-1-[(3,4-dichlorobenzyl)oxy]-1H-imidazo[4,5-b]pyridine 6-[(4-Chlorobenzyl)sulfanyl]imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime 2-(4-Chlorophenyl)-1-[(3,4-dichlorobenzyl)oxy]-1H-1,3-benzimidazole 1-(2,4-Dichlorobenzyl)-1H-indole-2,3-dione 3-[O-(3,4-dichlorobenzyl)oxime] 5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde O-(3,4-dichlorobenzyl)oxime N-(4-Chlorophenyl)-3-([(3,4-dichlorobenzyl)oxy]imino)propanamide 6-Chloro-1-[(3,4-dichlorobenzyl)oxy]-2-phenyl-1H-1,3-benzimidazole 5-[(4-Chlorophenyl)sulfanyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde O-(3,4-dichlorobenzyl)oxime 3-(4-Chlorophenyl)-3-oxopropanal O-(3,4-dichlorobenzyl)oxime