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IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID

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IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Basic information

Product Name:
IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
Synonyms:
  • IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
  • H-imidazo[1,2-a]pyridine-8-carboxylic acid
  • Imidazo[1,2-a]pyridine-8-...
  • 8-imidazo[1,2-a]pyridinecarboxylic acid
  • IMidazo[1,2-a]pyridin-8-carboxylic acid
  • H-iMidazo[1,2-a]pyridine-8-carbo×ylic acid
  • Imidazo[1,2-a]pyridine-8-carboxylicaci
  • IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID ISO 9001:2015 REACH
CAS:
133427-08-4
MF:
C8H6N2O2
MW:
162.15
Product Categories:
  • CHIRAL CHEMICALS
Mol File:
133427-08-4.mol
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IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Chemical Properties

Density 
1.41
storage temp. 
Sealed in dry,Room Temperature
pka
-0.61±0.41(Predicted)
form 
solid
color 
White
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-43
Safety Statements 
36/37
HS Code 
2933399990
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IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Usage And Synthesis

Synthesis

5345-47-1

7252-83-7

133427-08-4

General procedure for the synthesis of imidazo[1,2-a]pyridine-8-carboxylic acid from 2-aminonicotinic acid and 2-bromo-1,1-dimethoxyethane: To a suspension of 2-aminonicotinic acid (0.69 g, 5.00 mmol) in acetonitrile (20 mL) was added 2-bromo-1,1-dimethoxyethane (0.59 mL, 5.00 mmol). The resulting mixture was heated to 150 °C in a microwave reactor and kept for 2 hours. After completion of the reaction, the precipitate was collected by filtration and washed sequentially with acetonitrile and hexane to afford imidazo[1,2-a]pyridine-8-carboxylic acid (0.924 g) as a gray solid.

References

[1] Patent: WO2009/23253, 2009, A2. Location in patent: Page/Page column 52
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 5, p. 1870 - 1873

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