6-Bromo-2,3-dimethylimidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, which contribute to its aromatic properties. The presence of a bromine atom at the 6-position and two methyl groups at the 2 and 3 positions enhances its chemical reactivity and influences its physical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents. It is of interest in the field of medicinal chemistry and toxicology due to its potential role as a mutagen and carcinogen, particularly in relation to cooked meats where it can form during the cooking process of amino acids and creatine. The compound's structure allows for various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a valuable intermediate in synthetic organic chemistry. Additionally, its unique structure and reactivity profile make it a subject of study in understanding the mechanisms of carcinogenesis and the development of new pharmaceuticals.

6-bromo-2,3-dimethylimidazo[1,2-a]pyridine

121394-38-5: 6-Bromo-2,3-dimethylimidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, which contribute to its aromatic properties. The presence of a bromine atom at the 6-position and two methyl groups at the 2 and 3 positions enhances its chemical reactivity and influences its physical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents. It is of interest in the field of medicinal chemistry and toxicology due to its potential role as a mutagen and carcinogen, particularly in relation to cooked meats where it can form during the cooking process of amino acids and creatine. The compound's structure allows for various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a valuable intermediate in synthetic organic chemistry. Additionally, its unique structure and reactivity profile make it a subject of study in understanding the mechanisms of carcinogenesis and the development of new pharmaceuticals.

CAS 121394-38-5

6-bromo-2,3-dimethylimidazo[1,2-a]pyridine

6-Bromo-2,3-dimethylimidazo[1,2-a]pyridine

Ref: IN-DA009Y4F

6-Bromo-2,3-dimethylimidazo[1,2-a]pyridine

Ref: 3D-WEA39438