CAS 17969-26-5
:2-(3-Chlorophenyl)-4-thiazoleacetic acid
Description:
2-(3-Chlorophenyl)-4-thiazoleacetic acid is a chemical compound characterized by its thiazole and phenyl functional groups. It features a thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen, contributing to its unique reactivity and properties. The presence of the 3-chlorophenyl group enhances its lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water, which is common for many thiazole derivatives. Its acidic nature is attributed to the carboxylic acid functional group, allowing it to participate in various chemical reactions, including esterification and amidation. The compound may also exhibit biological activities, such as antimicrobial or anti-inflammatory properties, which are often investigated in drug development. Safety data should be consulted for handling and usage, as with all chemical substances, to ensure proper precautions are taken.
Formula:C11H8ClNO2S
InChI:InChI=1S/C11H8ClNO2S/c12-8-3-1-2-7(4-8)11-13-9(6-16-11)5-10(14)15/h1-4,6H,5H2,(H,14,15)
InChI key:InChIKey=CCUFHQQWZTVOCR-UHFFFAOYSA-N
SMILES:C(C(O)=O)C=1N=C(SC1)C2=CC(Cl)=CC=C2
Synonyms:- 2-(3-Chlorophenyl)-4-thiazoleacetic acid
- 2-[2-(3-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid
- 4-Thiazoleacetic acid, 2-(3-chlorophenyl)-
- 4-Thiazoleacetic acid, 2-(m-chlorophenyl)-
- Ici 55100
- [2-(3-Chloro-phenyl)-thiazol-4-yl]-acetic acid
- [2-(3-Chlorophenyl)-1,3-Thiazol-4-Yl]Acetate
- [2-(3-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid
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