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3,5-Dichloro-2-pyridinecarboxylic acid

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3,5-Dichloro-2-pyridinecarboxylic acid Basic information

Product Name:
3,5-Dichloro-2-pyridinecarboxylic acid
Synonyms:
  • 3,5-DICHLOROPYRIDINE-2-CARBOXYLIC ACID
  • 3,5-DICHLORO-2-PYRIDINECARBOXYLIC ACID
  • RARECHEM AL BO 2401
  • 3,5-Dichloropicolinic acid
  • 3,5-DICHLORO-2-PYRIDINECARBOXYLIC ACID 98+%
  • 3,5-Dichloropicolinic acid, 2-Carboxy-3,5-dichloropyridine
  • 2-Pyridinecarboxylicacid, 3,5-dichloro-
  • 3,5-Dichloro-2-pyridinecarboxylic acid ISO 9001:2015 REACH
CAS:
81719-53-1
MF:
C6H3Cl2NO2
MW:
192
Product Categories:
  • Heterocycle-Pyridine series
  • pharmacetical
  • Pyridine
  • API intermediates
  • Pyridines
  • Carboxylic Acids
Mol File:
81719-53-1.mol
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3,5-Dichloro-2-pyridinecarboxylic acid Chemical Properties

Melting point:
153-154 °C
Boiling point:
315.4±37.0 °C(Predicted)
Density 
1.612±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder
pka
2.12±0.25(Predicted)
color 
White
CAS DataBase Reference
81719-53-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
RIDADR 
UN2811
HazardClass 
IRRITANT
HS Code 
2933399990
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3,5-Dichloro-2-pyridinecarboxylic acid Usage And Synthesis

Synthesis

85331-33-5

81719-53-1

General procedure for the synthesis of 3,5-dichloro-2-pyridinecarboxylic acid from 2-cyano-3,5-dichloropyridine: 3,5-dichloro-2-pyridinecarbonitrile (10 g, 57.8 mmol) was dissolved in 100 mL of 95% concentrated sulfuric acid, and the reaction mixture was heated to 115 °C and kept reacting overnight. Upon completion of the reaction, the mixture was cooled to room temperature, followed by slow pouring into ice water and vigorous stirring. The precipitated solid product was collected by filtration, washed thoroughly with cold water and finally dried under reduced pressure at 40 °C to give 9.4 g of white solid product in 85% yield.

References

[1] Patent: WO2009/89263, 2009, A2. Location in patent: Page/Page column 117

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