ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Pyridine compound Pyridine derivatives Imidazo[1,2-a]pyridine

Imidazo[1,2-a]pyridine

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;1,3a-Diazaindene;IMidazo[1,2-a]pyridine 99%;N-[4-(4-nitrophenyl)sulfonylphenyl]-2-(1-piperidinyl)acetamide;Imidazo[1,2-a]pyridine>;Imidazo[1,2-a]pyridine ISO 9001：2015 REACH
CAS:274-76-0
MF:C7H6N2
MW:118.14
EINECS:
Product Categories:Building Blocks;C6 to C7;Chemical Synthesis;Heterocyclic Building Blocks;Imidazopyridines;C7 and C8;Heterocyclic Building Blocks;Pyridines
Mol File:274-76-0.mol
Imidazo[1,2-a]pyridine Structure
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.)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform, Methanol
form Powder
pka6.80±0.30(Predicted)
color White to off-white
λmax297nm(EtOH)(lit.)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
Imidazo[1,2-a]pyridine Usage And Synthesis
Chemical PropertiesYellow to Brown Oil
UsesImidazo[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.
UsesImidazo[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.
General DescriptionIn vivo anti-trypanosomal activity of imidazo[1,2-a]pyridiness in the STIB900 mouse model has been investigated.
Purification Methods1-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.]
Imidazo[1,2-a]pyridine Preparation Products And Raw materials
Preparation Products3-(4-Chlorophenyl)imidazo[1,2-a]pyridine
4-IMIDAZO[1,2-A]PYRIDIN-2-YL-PHENYLAMINE 2,7-DIMETHYLPYRIDO[1,6-A]-1H-IMIDAZOLE-3-CARBOXYLIC ACID, ETHYL ESTER ETHYL 2-PHENYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE 8-CHLORO-2-PHENYL-6-(TRIFLUOROMETHYL)IMIDAZO[1,2-A]PYRIDINE ETHYL 2,6-DIMETHYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE METHYL IMIDAZO[1,2-A]PYRIDINE-6-CARBOXYLATE N-(2,4-DIFLUOROPHENYL)-2,8-DIMETHYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXAMIDE ETHYL 6-METHYL-2-PHENYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE N-(4-FLUOROPHENYL)-2,7-DIMETHYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXAMIDE 2,7-DIMETHYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID 2-METHYL-N-(4-METHYLPHENYL)IMIDAZO[1,2-A]PYRIDINE-3-CARBOXAMIDE Chromium picolinate IMIDAZOPYRIDINE 2-[4-(DIFLUOROMETHOXY)PHENYL]IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE BUTTPARK 42\01-09 N-(4-CHLOROPHENYL)-2,8-DIMETHYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXAMIDE 2-(4-FLUOROPHENYL)IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID N-(4-CHLOROPHENYL)-2-METHYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXAMIDE
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