5-Methyl-4-thiazolemethanol is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen. This compound features a hydroxymethyl group (-CH2OH) attached to the thiazole, contributing to its reactivity and potential applications in various fields. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methyl group enhances its hydrophobic properties, while the hydroxymethyl group increases its polarity, allowing for diverse interactions in chemical reactions. 5-Methyl-4-thiazolemethanol may exhibit biological activity, making it of interest in pharmaceutical research and development. Its unique structure allows it to participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, this compound's distinctive features make it a subject of interest in both synthetic chemistry and potential applications in medicinal chemistry.

5-Methyl-4-thiazolemethanol

848774-94-7: 5-Methyl-4-thiazolemethanol is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen. This compound features a hydroxymethyl group (-CH2OH) attached to the thiazole, contributing to its reactivity and potential applications in various fields. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methyl group enhances its hydrophobic properties, while the hydroxymethyl group increases its polarity, allowing for diverse interactions in chemical reactions. 5-Methyl-4-thiazolemethanol may exhibit biological activity, making it of interest in pharmaceutical research and development. Its unique structure allows it to participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, this compound's distinctive features make it a subject of interest in both synthetic chemistry and potential applications in medicinal chemistry.

CAS 848774-94-7

5-Methyl-4-thiazolemethanol

(5-methyl-1,3-thiazol-4-yl)methanol

Ref: IN-DA004MLK

(5-methyl-1,3-thiazol-4-yl)methanol hydrochloride

Ref: 10-F360612