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CAS 4926-54-9

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5-bromo-3-methylimidazo[1,2-a]pyridine

Description:
5-Bromo-3-methylimidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, with a bromine atom and a methyl group substituent. This compound is known for its potential mutagenic properties, often studied in the context of food chemistry, particularly in cooked meats where it can form during the Maillard reaction. It exhibits a planar structure, which contributes to its ability to intercalate with DNA, potentially leading to genetic mutations. The presence of the bromine atom enhances its reactivity and can influence its biological activity. 5-Bromo-3-methylimidazo[1,2-a]pyridine is typically analyzed using techniques such as chromatography and mass spectrometry due to its complex structure. Its solubility is generally moderate in organic solvents, and it may exhibit varying degrees of stability depending on environmental conditions. Understanding its characteristics is crucial for assessing its implications in toxicology and carcinogenicity, as well as for developing strategies to mitigate its formation in food products.
Formula:C8H7BrN2
InChI:InChI=1/C8H7BrN2/c1-6-5-10-8-4-2-3-7(9)11(6)8/h2-5H,1H3
SMILES:Cc1cnc2cccc(Br)n12
Synonyms:
  • Imidazo[1,2-a]pyridine, 5-bromo-3-methyl-
  • 5-Bromo-3-methylimidazo[1,2-a]pyridine
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