5-Chloro-2-methylthiazolo[5,4-b]pyridine is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both thiazole and pyridine rings. This compound features a chlorine atom and a methyl group attached to the thiazole moiety, contributing to its chemical reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. The presence of the thiazole and pyridine rings suggests that it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, compounds of this class are often investigated for their pharmacological properties, as they may exhibit antimicrobial, anti-inflammatory, or anticancer activities. The chlorine substituent can influence the compound's lipophilicity and overall biological interactions. As with many heterocycles, the synthesis and characterization of 5-chloro-2-methylthiazolo[5,4-b]pyridine are of interest in medicinal chemistry and materials science.

5-chloro-2-methylthiazolo[5,4-b]pyridine

109202-21-3: 5-Chloro-2-methylthiazolo[5,4-b]pyridine is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both thiazole and pyridine rings. This compound features a chlorine atom and a methyl group attached to the thiazole moiety, contributing to its chemical reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. The presence of the thiazole and pyridine rings suggests that it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, compounds of this class are often investigated for their pharmacological properties, as they may exhibit antimicrobial, anti-inflammatory, or anticancer activities. The chlorine substituent can influence the compound's lipophilicity and overall biological interactions. As with many heterocycles, the synthesis and characterization of 5-chloro-2-methylthiazolo[5,4-b]pyridine are of interest in medicinal chemistry and materials science.

5-Chloro-2-methylthiazolo[5,4-b]pyridine

<p>5-Chloro-2-methyl-thiazolo[5,4-b]pyridine</p>

CAS 109202-21-3

5-chloro-2-methylthiazolo[5,4-b]pyridine

5-Chloro-2-methylthiazolo[5,4-b]pyridine

Ref: IN-DA007BBN

5-Chloro-2-methyl-thiazolo[5,4-b]pyridine

Ref: 54-OR314017

5-Chloro-2-methylthiazolo[5,4-b]pyridine

Ref: 10-F779329