ChemicalBook Product Catalog Chemical Reagents Organic reagents Phenols 2-Amino-5-chlorophenol

2-Amino-5-chlorophenol

2-Amino-5-chlorophenol Basic information
Product Name:2-Amino-5-chlorophenol
Synonyms:TIMTEC-BB SBB004137;4-CHLORO-2-HYDROXYANILINE;2-AMINO-5-CHLOROPHENOL;2-Amino-5-chlorophenol,99%;4-Chloro-2-hydroxyaniline, 97+%;2-Amino-5-chlorophenol ,97%;2-Amino-5-chlorophen;2-Amino-5-chlorophenol 97%
CAS:28443-50-7
MF:C6H6ClNO
MW:143.57
EINECS:249-020-3
Product Categories:Building Blocks;C6 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Organic Building Blocks;Oxygen Compounds;Phenols;Aromatic Phenols;Phenol&Thiophenol&Mercaptan;Phenoles and thiophenoles
Mol File:28443-50-7.mol
2-Amino-5-chlorophenol Structure
2-Amino-5-chlorophenol Chemical Properties
Melting point 145-153 °C (lit.)
Boiling point 185.5°C (rough estimate)
density 1.2028 (rough estimate)
vapor pressure 0.002-0.094Pa at 20-50℃
refractive index 1.5618 (estimate)
solubility soluble in Methanol
pka8.79±0.10(Predicted)
form Powder
color Light brown
CAS DataBase Reference28443-50-7(CAS DataBase Reference)
EPA Substance Registry SystemPhenol, 2-amino-5-chloro- (28443-50-7)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-36-36/37/39
WGK Germany 3
Hazard Note Irritant
TSCA Yes
HazardClass 6.1
HS Code 29222990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
2-Amino-5-chlorophenol Usage And Synthesis
Chemical Propertieslight brown fine crystalline powder
Uses2-Amino-5-chlorophenol may be used to synthesize 2-amino-5-chloromuconic semialdehyde and benzoxazole derivatives.
DefinitionChEBI: Phenol carrying amino and chloro substituents at positions 2 and 5 respectively. It is part of the degradation pathway of 4-chloronitrobenzene, CHEBI:34399.
General Description2-Amino-5-chlorophenol can be synthesized from 2-chloro-5-nitrophenol via reduction. It can also be obtained from 1-chloro-4-nitrobenzene by using a bacterial strain LW1. 2-Amino-5-chlorophenol participates in the condensation reaction with acetylferrocene to afford ferrocenyl Schiff bases bearing a phenol group.
2-Amino-5-chlorophenol Preparation Products And Raw materials
Preparation Products4-CHLORO-2-ANISIDINE HYDROCHLORIDE-->2,6-Dichlorobenzoxazole-->6-Chloro-2-benzoxazolethiol
3-amino-2-chlorophenol 4'-Chloro-2',5'-dimethoxyacetoacetanilide 4-AMINO-3-CHLOROPHENOL 2-amino-4-chlorophenol-5-sulfo,2-AMINO-4-CHLOROPHENOL-5-SULFONAMIDE 1-CHLORO-2,5-DIETHOXY-4-NITROBENZENE 2-Amino-6-chlorophenol-4-sulfonic acid 6-Amino-4-chlorophenol-2-sulfonic acid,2-AMINO-4-CHLOROPHENOL-6-SULFONIC ACID 2-Methyl-5-amino-4-chlorophenol 3-AMINO-5-CHLOROPHENOL CHLOROPHENOL N-(4-Chloro-3-hydroxyphenyl)acetamide ALTRENOGEST 5-AMINO-2-CHLOROPHENOL,3-amino-6-chloropheno DICLOFENAC ACID 4-Chloro-2-methoxy-N-methylaniline 96% 1-Chloro-2,5-dimethoxy-4-nitrobenzene AMINO ACIDS 5-CHLORO-2-NITROANISOLE
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