4-Amino-3-chlorophenol

4-Amino-3-chlorophenol

Product Introduction

4-Amino-3-chlorophenol Basic information
Product Name: 4-Amino-3-chlorophenol
Synonyms: AMINO(4-)-3-CHLOROPHENOL;4-AMINO-3-CHLOROPHENOL;3-chloro-4-aminophenol;4-amino-3-chloro-pheno;Brn 2802558;Einecs 241-583-3;Phenol, 4-amino-3-chloro-;lenvaint-G
CAS: 17609-80-2
MF: C6H6ClNO
MW: 143.57
EINECS: 241-583-3
Product Categories: 17609-80-2
Mol File: 17609-80-2.mol
4-Amino-3-chlorophenol Structure
 
4-Amino-3-chlorophenol Chemical Properties
Melting point 159-160℃
Boiling point 287.3±25.0 °C(Predicted)
density 1.406±0.06 g/cm3(Predicted)
RTECS SJ5710000
storage temp. 2-8°C(protect from light)
solubility DMSO (Slightly), Methanol (Slightly)
pka 9.26±0.18(Predicted)
form Crystalline Powder
color White
Stability: Hygroscopic
CAS DataBase Reference 17609-80-2(CAS DataBase Reference)
 
Safety Information
HazardClass 6.1
HS Code 2922290090
 
MSDS Information
 
 
4-Amino-3-chlorophenol Usage And Synthesis
Chemical Properties Light yellow solid
Uses 4-Amino-3-Chlorophenol acts as a synthetic reagent for the preparation of Benzothiazole-based ureas as potential ABAD/17β-HSD10 modulators for Alzheimer''s disease treatment.
Application The 4-amino-3-chlorophenol is a crucial intermediate for preparing a tyrosine kinase inhibitor, tivozanib, and a late liver cancer drug, lenvatinib. As a crucial pharmaceutical chemical intermediate, 4-amino-3-chlorophenol is widely applied to the design and synthesis of medicaments for resisting tumors, cardiovascular diseases, neurological diseases, and the like.
Synthesis Starting from o-chloronitrobenzene with introducing hydroxyl groups in the presence of strong acids and molybdenum salts as catalysts could synthesize 4-amino-3-chlorophenol. Besides, using m-chlorophenol as a starting material and introducing hydroxyl on a benzene ring through diazotization and coupling also could synthesize 4-Amino-3-chlorophenol.
 
4-Amino-3-chlorophenol Preparation Products And Raw materials
Preparation Products 2-Chloro-4-((5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yl)oxy)aniline-->tert-butyl 2-chloro-4-hydroxyphenylcarbamate

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