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ProductsDetails

Product Name:
Methyl (S)-3-(4-bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoate
CAS No:
2641451-73-0
EC No:
-
Synonyms:
2-Thiazolepropanoic acid, 4-bromo-α-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester, (αS)-;Methyl (S)-2-(Boc-amino)-3-(4-bromo-2-thiazolyl)propanoate; Methyl (S)-3-(4-bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoate,2641451-73-0,2-Thiazolepropanoic acid 4-bromo-α-[[(1,1-dimethylethoxy)carbonyl]amino]- methyl ester (αS)-,Boc-L-3-(4-bromothiazol-2-yl)alanine methyl ester,Suzhou Health Chemicals Co. Ltd.,Chiral pharmaceutical intermediates,Thiazole building blocks,Non-natural amino acid derivatives,Boc protected amino acid esters,Chemical synthesis building blocks,High purity pharma intermediates,Pharma raw materials supplier China,Custom synthesis building blocks,CAS 2641451-73-0 supplier,API intermediate manufacturing 2641451-73-0,Methyl (S)-3-(4-bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoate,Chiral Pharmaceutical Intermediate,Thiazole Building Blocks,Suzhou Health Chemicals

Product Introduction

Methyl (S)-3-(4-bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoate serves as an advanced non-natural chiral amino acid derivative and pharmaceutical intermediate. It is primarily utilized in building the structural frameworks of novel small-molecule targeted therapeutics, anti-cancer agents, antivirals, and bioactive peptidomimetics. The highly reactive bromothiazole ring in its molecule facilitates diverse functionalization via Suzuki, Stille, or Buchwald coupling reactions. Meanwhile, its defined chiral center guarantees stereospecific synthesis for peptide-based drug discovery, making it a vital chemical building block for pharmaceutical R&D and commercial lead optimization.

RMC-6236 intermediate; Daraxonrasib intermediate



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