Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  Phenol derivatives >  4-Amino-2,3-dichlorphenol

4-Amino-2,3-dichlorphenol

Basic information Safety Supplier Related

4-Amino-2,3-dichlorphenol Basic information

Product Name:
4-Amino-2,3-dichlorphenol
Synonyms:
  • 4-Amino-2,3-dichlorphenol
  • 4-AMino-2,3-dichlorophenol
  • Phenol,4-amino-2,3-dichloro-
  • Lenvatinib Impurity 88
  • 4-hydroxy-2,3-dichloroaniline
  • Lenvatinib Impurity 110
  • 2,3-dichloro-4-hydroxyaniline
  • Glucosamine Hydrochloride Impurity 17
CAS:
39183-17-0
MF:
C6H5Cl2NO
MW:
178.02
Product Categories:
  • john's
Mol File:
39183-17-0.mol
More
Less

4-Amino-2,3-dichlorphenol Chemical Properties

Melting point:
>129°C (dec.)
Boiling point:
301.9±42.0 °C(Predicted)
Density 
1.560±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO, Methanol
pka
7.81±0.23(Predicted)
form 
Solid
color 
Brown
More
Less

Safety Information

HS Code 
2922290090
More
Less

4-Amino-2,3-dichlorphenol Usage And Synthesis

Uses

4-Amino-2,3-dichlorophenol is used in the synthesis of Fenhexamid and other pyrazine compounds for use in drug formulations in treating inflammation, respiratory disorders and viral infections.

Synthesis

201656-71-5

39183-17-0

To a 100 mL two-necked flask equipped with a stirrer and reflux condenser was added 8.0 g (0.03 mol) of 2,3-dichloro-4-phenylazophenol (CAS: 201656-71-5) and 1 g of sodium hydroxide dissolved in 40 mL of ethanol. The reaction system was cooled in an ice-water bath, followed by the addition of 4.5 g (0.12 mol) of sodium borohydride in one drop. After the dropwise addition was completed, the ice bath was removed and the reaction mixture was gradually warmed up to room temperature and the reaction was continued with stirring for 4 hours. Upon completion of the reaction, the pH of the reaction solution was adjusted to 7 with dilute hydrochloric acid solution and then extracted three times with ethyl acetate. The organic phases were combined, dried with anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure. The crude product was recrystallized with 20 mL of toluene, and after filtration and drying, 5.08 g of light pink crystalline 4-amino-2,3-dichlorophenol was obtained in 95% yield and 100% purity.

References

[1] Patent: CN105732403, 2016, A. Location in patent: Paragraph 0038; 0039; 0040

4-Amino-2,3-dichlorphenolSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Shanghai Synmedia Chemical Co., Ltd.
Tel
021-38681880 13817889927
Email
sales@synmedia-chem.com
Bide Pharmatech Ltd.
Tel
400-400-164-7117 18317119277
Email
product02@bidepharm.com
Quality Control Solutions Ltd.
Tel
66853366 13670046396
Email
sales@chem-strong.com