4-Chloro-2-methyl-oxazolo[5,4-c]pyridine is a heterocyclic compound characterized by its fused oxazole and pyridine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 4-position and a methyl group at the 2-position of the oxazole ring influences its reactivity and solubility. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with heterocyclic compounds. The chlorine substituent can enhance lipophilicity, potentially affecting the compound's interaction with biological targets. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile building block in organic synthesis. As with many heterocycles, it may also exhibit interesting electronic properties, which can be explored in materials science and organic electronics.

4-chloro-2-methyl-oxazolo[5,4-c]pyridine

1354831-15-4: 4-Chloro-2-methyl-oxazolo[5,4-c]pyridine is a heterocyclic compound characterized by its fused oxazole and pyridine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 4-position and a methyl group at the 2-position of the oxazole ring influences its reactivity and solubility. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with heterocyclic compounds. The chlorine substituent can enhance lipophilicity, potentially affecting the compound's interaction with biological targets. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile building block in organic synthesis. As with many heterocycles, it may also exhibit interesting electronic properties, which can be explored in materials science and organic electronics.

CAS 1354831-15-4

4-chloro-2-methyl-oxazolo[5,4-c]pyridine

4-Chloro-2-methyloxazolo[5,4-c]pyridine

Ref: IN-DA00AAPV

4-Chloro-2-methyl[1,3]oxazolo[5,4-c]pyridine

Ref: 54-OR305553