(2-Chloro-1,3-thiazol-5-yl)methanol is a chemical compound characterized by its thiazole ring, which contains both sulfur and nitrogen atoms, contributing to its unique reactivity and properties. The presence of a chlorine atom at the 2-position of the thiazole ring enhances its electrophilic character, making it potentially useful in various chemical reactions, including nucleophilic substitutions. The methanol group (-CH2OH) attached to the thiazole provides the compound with hydroxyl functionality, which can participate in hydrogen bonding and increase its solubility in polar solvents. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structural features suggest potential applications in agrochemicals or as intermediates in organic synthesis. Additionally, the compound's stability, reactivity, and solubility can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial settings. Overall, (2-chloro-1,3-thiazol-5-yl)methanol is a versatile compound with significant implications in various fields of chemistry.

(2-chloro-1,3-thiazol-5-yl)methanol

145015-15-2: 5-Thiazolemethanol, 2-chloro-, (2-Chloro-1,3-thiazol-5-yl)methanol

5-Thiazolemethanol, 2-chloro-

CAS 145015-15-2: (2-chloro-1,3-thiazol-5-yl)methanol

5-Thiazolemethanol, 2-chloro-

Ref: IN-DA001KHJ

2-Chloro-5-(hydroxymethyl)-1,3-thiazole

Ref: 54-OR8406

(2-Chloro-1,3-thiazol-5-yl)methanol

Ref: 3D-VFA01515

2-Chloro-5-hydroxymethylthiazole

Ref: 10-F016116