Ethyl 2-[2-isobutoxy-5-(5-methoxycarbonyl-4-methyl-1,3-thiazol-2-yl)phenyl]-4-methyl-1,3-thiazole-5-carboxylate

CAS No. : NA
Mol F. : C23H26N2O5S2
Mol W. : 474.6
Cat No. : SA32021
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Description

Product Name Ethyl 2-[2-isobutoxy-5-(5-methoxycarbonyl-4-methyl-1,3-thiazol-2-yl)phenyl]-4-methyl-1,3-thiazole-5-carboxylate
Synonyms 2-(3-(5-(ethoxycarbonyl)-4-methylthiazol-2-yl)-4-isobutoxyphenyl-4-methylthiazole-5-carboxylic acid methylester

Related API Febuxostat
Category Impurities

Ethyl 2-[2-isobutoxy-5-(5-methoxycarbonyl-4-methyl-1,3-thiazol-2-yl)phenyl]-4-methyl-1,3-thiazole-5-carboxylate product with CAS: NA is also known as 2-(3-(5-(ethoxycarbonyl)-4-methylthiazol-2-yl)-4-isobutoxyphenyl-4-methylthiazole-5-carboxylic acid methylester; . This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Febuxostat and its related formulations. Moreover, 2-(3-(5-(ethoxycarbonyl)-4-methylthiazol-2-yl)-4-isobutoxyphenyl-4-methylthiazole-5-carboxylic acid methylester is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other impurities of Febuxostat developed in our R&D.

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Certificate of Analysis (CoA) and Characterization Data:

All products are provided with a certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS, etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply). 

This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This product provided by SynThink is generally used for Abbreviated New Drug Application (ANDA) filing to FDA, toxicity study of respective drug formulation, Quality Control (QC) and analytical studies during commercial production of the API]. Please also find out process impurities, degradation impurities, potential impurities of related api/drug developed by our R&D.

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