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Structure of 2641451-74-1
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(S)-3-(4-Bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid features a chiral α-amino acid scaffold bearing a brominated thiazole heterocycle and a stable tert-butoxycarbonyl (Boc) protecting group. This configuration enables direct incorporation into peptide synthesis workflows, where the electron-deficient thiazole enhances structural rigidity and facilitates downstream functionalization. The Boc moiety ensures compatibility with standard deprotection protocols.
(S)-3-(4-Bromothiazol-2-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a versatile chiral building block for the synthesis of thiazole-containing peptidomimetics and bioactive heterocycles. The Boc-protected amino group enables straightforward deprotection and coupling in peptide synthesis, while the 4-bromothiazole moiety supports palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to complex scaffolds in medicinal chemistry and process development.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: