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Sku CI17129_5_G
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Product Information

Product Name
Thiazole-5-carboxylic acid
Brand Name
Chem Impex
Product Number
17129
CAS
14527-41-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
84494
IUPAC Name
1,3-thiazole-5-carboxylic acid
InChI Key
YZVFSQQHQPPKNX-UHFFFAOYSA-N
SMILES
C1=C(SC=N1)C(=O)O

Application

Thiazole-5-carboxylic acid is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly those targeting bacterial infections and cancer. Its unique structure allows for the development of novel drug candidates with improved efficacy.

Agricultural Chemistry: It is used in the formulation of agrochemicals, including fungicides and herbicides. The compound's ability to inhibit specific enzymes makes it effective in protecting crops from pests and diseases.

Material Science: Thiazole-5-carboxylic acid is employed in the production of specialty polymers and resins. These materials often exhibit enhanced thermal stability and mechanical properties, making them suitable for high-performance applications.

Analytical Chemistry: The compound is utilized as a reagent in various analytical techniques, including chromatography and spectroscopy. Its ability to form stable complexes with metal ions aids in the detection and quantification of trace elements in samples.

Biochemistry Research: It plays a role in the study of metabolic pathways and enzyme activity. Researchers use it to explore the biochemical mechanisms underlying various physiological processes, contributing to advancements in health sciences.

References Data Source From Pubchem

Bisprenyl naphthoquinone and chlorinated calcimycin congener bearing thiazole ring from an actinomycete of the genus Phytohabitans

Publication Name: The Journal of Antibiotics
Publication Date: 2022-09-07
DOI: 10.1038/s41429-022-00559-x

Copper coordination polymers constructed from thiazole-5-carboxylic acid: Synthesis, crystal structures, and structural transformation

Publication Name: Journal of Solid State Chemistry
Publication Date: 2017-01
DOI: 10.1016/j.jssc.2016.10.009

Transition Metal-Catalyzed Decarboxylation and Decarboxylative Cross-Couplings

Publication Name: New Carbon–Carbon Coupling Reactions Based on Decarboxylation and Iron-Catalyzed C–H Activation
Publication Date: 2016-12-11
DOI: 10.1007/978-981-10-3193-9_1

Polymorphism in metal complexes of thiazole-4-carboxylic acid

Publication Name: Transition Metal Chemistry
Publication Date: 2016-07-26
DOI: 10.1007/s11243-016-0079-7