4-Methyl-5-thiazolyl methanol is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound features a hydroxymethyl group (-CH2OH) attached to the thiazole ring, contributing to its reactivity and potential applications in various chemical reactions. The presence of the methyl group at the 4-position of the thiazole enhances its lipophilicity, which can influence its biological activity and solubility in organic solvents. 4-Methyl-5-thiazolyl methanol is often studied for its potential pharmacological properties, including antimicrobial and antifungal activities, making it of interest in medicinal chemistry. Additionally, its unique structure allows for various synthetic modifications, which can lead to the development of new derivatives with enhanced properties. As with many thiazole derivatives, it may also exhibit interesting interactions with biological targets, warranting further investigation into its mechanisms of action and potential therapeutic applications.

4-METHYL-5-THIAZOLYL METHANOL

1977-06-6: (4-Methyl-1,3-thiazol-5-yl)methanol, 5-Thiazolemethanol, 4-Methyl-

5-Thiazolemethanol, 4-methyl-

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

4-Methylthiazol-5-yl)methanol is a synthetic reducer that has been shown to have antibacterial properties. It is used in the postprocessing of chronic bronchitis and has been shown to reduce exacerbations. 4-Methylthiazol-5-yl)methanol is also an oxidising agent, which can be used in the treatment of acute bronchitis. 4-Methylthiazol-5-yl)methanol reacts with chloride ions and organic substances to form a chloride salt and an organic substance. This reaction yield depends on the concentration of chloride ions present, as well as the concentration of organic solvent. The product is then hydrolysed by pgf2α to form a fatty acid. 4-Methylthiazol-5-yl)methanol is also involved in oxidative stress responses and mediates inflammatory responses through its ability to inhibit phosphodiesterase activity.

CAS 1977-06-6: 4-METHYL-5-THIAZOLYL METHANOL

5-Thiazolemethanol, 4-methyl-

Ref: IN-DA002AYU

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

Ref: 54-OR937622

(4-Methylthiazol-5-yl)methanol

Ref: 3D-BAA97706

(4-Methylthiazol-5-yl)methanol

Ref: 10-F217920