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Imidazo[1,2-a]pyridine

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Imidazo[1,2-a]pyridine Basic information

Product Name:
Imidazo[1,2-a]pyridine
Synonyms:
  • IMIDAZO[1,2-A]PYRIDINE
  • 1-Azaindolizine
  • Pyridino[1',2':1,2]glyoxaline
  • Pyrimidazole
  • 1,3a-Diazaindene
  • IMidazo[1,2-a]pyridine 99%
  • N-[4-(4-nitrophenyl)sulfonylphenyl]-2-(1-piperidinyl)acetamide
  • Imidazo[1,2-a]pyridine>
CAS:
274-76-0
MF:
C7H6N2
MW:
118.14
Product Categories:
  • Building Blocks
  • C6 to C7
  • C7 and C8
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Imidazopyridines
  • Heterocyclic Building Blocks
  • Pyridines
Mol File:
274-76-0.mol
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Imidazo[1,2-a]pyridine Chemical Properties

Boiling point:
103 °C1 mm Hg(lit.)
Density 
1.165 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.626(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform, Methanol
pka
6.80±0.30(Predicted)
form 
Powder
color 
White to off-white
λmax
297nm(EtOH)(lit.)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900

MSDS

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Imidazo[1,2-a]pyridine Usage And Synthesis

Chemical Properties

Yellow to Brown Oil

Uses

Imidazo[1,2-a]pyridine is one of four imidazopyridine isomers. Imidazopyridine derivatives possess activity as inhibitors of target enzymes and have medicinal and pharmaceutical applications and are used as herbicides and fungicides.

Uses

Imidazo[1,2-a]pyridine is one of four imidazopyridine isomers. Imidazopyridine derivatives possess activity as inhibitors of target enzymes and have medicinal and pharmaceutical applications and are u sed as herbicides and fungicides.

General Description

In vivo anti-trypanosomal activity of imidazo[1,2-a]pyridiness in the STIB900 mouse model has been investigated.

Purification Methods

1-Azaindolizine is purified by distillation or gas chromatography. [Bower & Ramage J Chem Soc 4506 1957, Armarego J Chem Soc 4226 1964, Beilstein 23 II 1554, 23 III/IV 1104.]

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