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3-Chloroisonicotinic acid

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3-Chloroisonicotinic acid Basic information

Product Name:
3-Chloroisonicotinic acid
Synonyms:
  • 3-CHLOROISONICOTINIC ACID
  • 3-CHLOROPYRIDINE-4-CARBOXYLIC ACID
  • 3-CHLORO-4-PYRIDINECARBOXYLIC ACID
  • 3-Chloro-4-pyridine carboxlic acid
  • 3-Chloro-4-pyridinecarboxylic acid, 3-Chloroisonicotinic acid
  • 4-Pyridinecarboxylic acid, 3-chloro-
  • 3-Chloropyridine-4-carboxylic acid, 4-Carboxy-3-chloropyridine
  • 3- chlorineisonicotinic acid
CAS:
88912-27-0
MF:
C6H4ClNO2
MW:
157.55
Product Categories:
  • Pyridines
  • Pyridine
  • pharmacetical
  • Building Blocks
  • Carboxy
Mol File:
88912-27-0.mol
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3-Chloroisonicotinic acid Chemical Properties

Melting point:
227-231 °C (dec.)(lit.)
Boiling point:
387.0±22.0 °C(Predicted)
Density 
1.470±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
0.12±0.25(Predicted)
form 
Solution
color 
Brown to dark green to black
InChIKey
MYAZXWFEMDJTFE-UHFFFAOYSA-N
CAS DataBase Reference
88912-27-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22
Safety Statements 
36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29333999

MSDS

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3-Chloroisonicotinic acid Usage And Synthesis

Synthesis

626-60-8

88912-27-0

A. Synthesis of 3-chloro-N-(4-chlorophenyl)pyridine-4-carboxamide. At -78 °C, 3-chloropyridine (1.00 mL, 10.5 mmol) was dissolved in THF and a freshly prepared lithium diisopropylammonium THF solution [prepared by the reaction of butyl lithium (7.21 mL, 11.5 mmol) with diisopropylamine (11.5 mmol)] was slowly added. After 0.25 h of reaction, carbon dioxide gas was passed into the mixture and slowly warmed to room temperature. After completion of the reaction, the mixture was concentrated and subsequently partitioned between EtOAc and water. The aqueous layer was washed twice with EtOAc. The pH of the aqueous layer was adjusted to about 3 by adding 1N HCl and extracted three more times with EtOAc. The organic phases were combined, dried with magnesium sulfate and concentrated. The residue was recrystallized by EtOAc to give 200 mg (12% yield) of 3-chloroisonicotinic acid.

References

[1] Patent: US6610704, 2003, B1

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