2-(4-Chloro-1,3-thiazol-2-yl)acetic acid is a chemical compound characterized by its thiazole ring, which contains a chlorine substituent at the para position. This compound features an acetic acid functional group, contributing to its acidic properties. It is typically a solid at room temperature and is soluble in polar solvents due to the presence of the carboxylic acid group. The thiazole moiety imparts unique biological activity, making it of interest in pharmaceutical research, particularly for its potential antimicrobial and antifungal properties. The presence of chlorine enhances its reactivity and may influence its interaction with biological targets. As with many thiazole derivatives, it may exhibit a range of biological activities, making it a valuable compound in medicinal chemistry. Safety data should be consulted for handling, as with any chemical, to ensure proper precautions are taken due to potential toxicity or environmental impact.

2-(4-chloro-1,3-thiazol-2-yl)acetic acid

29676-72-0: 2-(4-Chloro-1,3-thiazol-2-yl)acetic acid is a chemical compound characterized by its thiazole ring, which contains a chlorine substituent at the para position. This compound features an acetic acid functional group, contributing to its acidic properties. It is typically a solid at room temperature and is soluble in polar solvents due to the presence of the carboxylic acid group. The thiazole moiety imparts unique biological activity, making it of interest in pharmaceutical research, particularly for its potential antimicrobial and antifungal properties. The presence of chlorine enhances its reactivity and may influence its interaction with biological targets. As with many thiazole derivatives, it may exhibit a range of biological activities, making it a valuable compound in medicinal chemistry. Safety data should be consulted for handling, as with any chemical, to ensure proper precautions are taken due to potential toxicity or environmental impact.

4-Thiazoleacetic acid, 2-chloro-

<p>Organic compound (4-Chloro-thiazol-2-yl)acetic acid aids protein folding, enzyme inhibition, and signal transduction research.</p>

CAS 29676-72-0

2-(4-chloro-1,3-thiazol-2-yl)acetic acid

4-Thiazoleacetic acid, 2-chloro-

Ref: IN-DA002Z21

(4-Chloro-thiazol-2-yl)acetic acid

Ref: TM-T4402

(4-Chlorothiazol-2-yl)acetic acid

Ref: 54-OR1020731

(4-CHLORO-THIAZOL-2-YL)ACETIC ACID

Ref: 10-F468284

(4-Chloro-thiazol-2-yl)acetic acid

Ref: 3D-EBA67672