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Structure of 2641451-73-0
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(S)-Methyl 3-(4-bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoate features a chiral center flanked by a bromothiazole moiety and a Boc-protected amine, enabling direct incorporation into peptide-like scaffolds. This bench-stable building block facilitates synthesis of bioactive heterocyclic compounds under standard conditions.
(S)-Methyl 3-(4-bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoate serves as a versatile chiral building block for the synthesis of thiazole-containing peptidomimetics and bioactive heterocycles. The protected amino group enables orthogonal deprotection, while the bromothiazole moiety supports palladium-catalyzed cross-coupling reactions. Bench-stable and readily purified by standard chromatography, it facilitates efficient access to complex scaffolds in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: