2-Chlorobenzyl alcohol

2-Chlorobenzyl alcohol Basic information
Product Name:2-Chlorobenzyl alcohol
Synonyms:Benzenemethanol,2-chloro-;Benzyl alcohol, o-chloro-;o-chlorobenzoylalcohol;ortho-Chlorobenzyl alcohol;o-Chlorobenzyl Alcohol 2-Chlorobenzyl Alcohol;2-Chlorobenzyl alcohol 98%;2-Chlorobenzenemehtanol;2-Chlorobenzyl alcohol,99%
CAS:17849-38-6
MF:C7H7ClO
MW:142.58
EINECS:241-801-7
Product Categories:Building Blocks;C6 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Aromatics;Benzhydrols, Benzyl & Special Alcohols;Alcohol;Alcohols;Chlorine Compounds;Organic Building Blocks;Oxygen Compounds;Phenols
Mol File:17849-38-6.mol
2-Chlorobenzyl alcohol Structure
2-Chlorobenzyl alcohol Chemical Properties
Melting point 69-71 °C (lit.)
Boiling point 227 °C (lit.)
density 1.1104 (rough estimate)
refractive index 1.5390 (estimate)
Fp 227°C
storage temp. Sealed in dry,Room Temperature
solubility chloroform: soluble25mg/mL, clear, colorless
pka13.99±0.10(Predicted)
form Fine Crystalline Powder
color White
BRN 2042182
LogP1.770
CAS DataBase Reference17849-38-6(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenemethanol, 2-chloro-(17849-38-6)
EPA Substance Registry System2-Chlorobenzenemethanol (17849-38-6)
Safety Information
Hazard Codes Xi
Safety Statements 22-24/25
WGK Germany 3
Hazard Note Irritant
HS Code 29062900
MSDS Information
ProviderLanguage
o-Chlorobenzyl alcohol English
SigmaAldrich English
ACROS English
ALFA English
2-Chlorobenzyl alcohol Usage And Synthesis
Chemical Propertieswhite fine crystalline powder
Uses(2-Chlorophenyl)methanol is used as a reactant in the preparation of aldehydes and ketones using transition metal free aerobic oxidation and catalyzed by TEMPO/Br2/NaNO2.
Synthesis Reference(s)Journal of the American Chemical Society, 69, p. 2548, 1947 DOI: 10.1021/ja01202a082
Synthetic Communications, 25, p. 1689, 1995 DOI: 10.1080/00397919508015853
General DescriptionMajor urinary metabolites of 2-chlorobenzyl alcohol in rats were 2-chlorohippuric acid, 2-chlorobenzyl cysteine, 2-chlorobenzoic acid and 2-chlorobenzyl glucuronic acid. It is a possible intermediate formed during the metabolism of 2-chloromandelic acid.
(R)-α-Methyl-4-chlorobenzyl alcohol 2-AMINO-5-CHLOROBENZYL ALCOHOL 4-BENZYLOXY-2-CHLOROBENZYL ALCOHOL 3-CHLOROBENZYL ALCOHOL [METHYLENE-14C] 3-Chlorobenzyl alcohol 98%,M-CHLOROBENZYL ALCOHOL,3-CHLOROBENZYL ALCOHOL 2-AMINO-5-CHLOROBENZYL ALCOHOL (+)-a-Aminomethyl-o-chlorobenzyl alcohol Chlorophenyl (S)-α-Methyl-3-chlorobenzyl alcohol alpha-[(tert-butylamino)methyl]-o-chlorobenzyl alcohol hydrochloride α-[2,2-Bis(methylthio)vinyl]-4-chlorobenzyl alcohol α-Methyl-4-chlorobenzyl alcohol α-Cyclopropyl-α-methyl-4-chlorobenzyl alcohol α-(2-Pyridyl)-α-(4-chlorophenyl)-4-chlorobenzyl alcohol chlorobenzyl alcohol 2-BROMO-5-CHLOROBENZYL ALCOHOL 2-(Chloromethyl)benzonitrile α-[(Benzylethylamino)methyl]-4-chlorobenzyl alcohol

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