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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  5-Chloro-1H-indazole-3-carboxylic acid

5-Chloro-1H-indazole-3-carboxylic acid

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5-Chloro-1H-indazole-3-carboxylic acid Basic information

Product Name:
5-Chloro-1H-indazole-3-carboxylic acid
Synonyms:
  • 5-CHLORO-1H-INDAZOLE-3-CARBOXYLIC ACID
  • 5-CHLORO-3-(1H)INDAZOLE CARBOXYLIC ACID
  • 5-CHLORO-3-INDAZOLECARBOXYLIC ACID
  • 5-CHLORO-3-INDOZOLE-CARBOXYLIC ACID
  • 1H-Indazole-3-carboxylic acid, 5-chloro-
  • 5-chloro-1H-indazol-3-carboxylic acid
  • 5-Chloro-1H-indazole-3-carboxylic acid ,97%
  • 5-chloro-1h-indazole-3-carboxylic acod
CAS:
1077-95-8
MF:
C8H5ClN2O2
MW:
196.59
Product Categories:
  • pharmacetical
  • Indazole
Mol File:
1077-95-8.mol
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5-Chloro-1H-indazole-3-carboxylic acid Chemical Properties

Melting point:
337 °C
Boiling point:
472.1±25.0 °C(Predicted)
Density 
1.644±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
2.82±0.30(Predicted)
color 
Yellow
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Safety Information

Risk Statements 
22-36
Safety Statements 
26
HS Code 
29339900
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5-Chloro-1H-indazole-3-carboxylic acid Usage And Synthesis

Chemical Properties

Light yellow solid

Synthesis

1H-indazole-3-carboxylic acid was dissolved in anhydrous acetic acid in a three-necked flask, heated and stirred. After the substrate was dissolved and clarified, phosphorus oxychloride was dissolved in anhydrous acetic acid and slowly added dropwise. In an oil bath at 90°C, the mixture was condensed back into the chemical book and reacted for 14 hours. After the reaction was complete, a white precipitate was produced. It was cooled in an ice bath, vacuum filtered, and the solid was washed with ethyl acetate first and then with ether to obtain 5-Chloro-1H-indazole-3-carboxylic acid.

5-Chloro-1H-indazole-3-carboxylic acid Preparation Products And Raw materials

Raw materials

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