6-Methyl[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic compound characterized by its fused triazole and pyridine rings, which contribute to its unique chemical properties. The presence of a methyl group at the 6-position of the triazole ring enhances its lipophilicity and can influence its biological activity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents, such as ethanol and dimethyl sulfoxide, but may have limited solubility in water. Its structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The compound may also exhibit various pharmacological activities, including antimicrobial and anti-inflammatory properties, although specific biological data may vary. As with many heterocycles, it can participate in diverse chemical reactions, including nucleophilic substitutions and cycloadditions, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and usage, as with any chemical substance.

6-methyl[1,2,4]triazolo[1,5-a]pyridine

4931-24-2: 6-Methyl[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic compound characterized by its fused triazole and pyridine rings, which contribute to its unique chemical properties. The presence of a methyl group at the 6-position of the triazole ring enhances its lipophilicity and can influence its biological activity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents, such as ethanol and dimethyl sulfoxide, but may have limited solubility in water. Its structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The compound may also exhibit various pharmacological activities, including antimicrobial and anti-inflammatory properties, although specific biological data may vary. As with many heterocycles, it can participate in diverse chemical reactions, including nucleophilic substitutions and cycloadditions, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and usage, as with any chemical substance.

CAS 4931-24-2

6-methyl[1,2,4]triazolo[1,5-a]pyridine

6-Methyl[1,2,4]triazolo[1,5-a]pyridine

Ref: IN-DA00DK49

6-Methyl-[1,2,4]triazolo[1,5-a]pyridine

Ref: 54-OR86004

6-Methyl-[1,2,4]triazolo[1,5-a]pyridine

Ref: 10-F634951