| Identification | Back Directory | [Name]
4-Amino-2,3-dichlorphenol | [CAS]
39183-17-0 | [Synonyms]
Lenvatinib Impurity 88
Lenvatinib Impurity 110
4-Amino-2,3-dichlorphenol
4-AMino-2,3-dichlorophenol
Phenol,4-amino-2,3-dichloro-
4-hydroxy-2,3-dichloroaniline
2,3-dichloro-4-hydroxyaniline
Glucosamine Hydrochloride Impurity 17 | [Molecular Formula]
C6H5Cl2NO | [MOL File]
39183-17-0.mol | [Molecular Weight]
178.02 |
| Chemical Properties | Back Directory | [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 | [form ]
Solid | [pka]
7.81±0.23(Predicted) | [color ]
Brown |
| Hazard Information | Back Directory | [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]
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 |
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Rhawn Reagent
|
| Telephone: |
400-400-1332688 18019345275 |
| Website: |
http://www.rhawn.cn |
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