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Structure of 89336-46-9
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This thiazole-based amino acid derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid group, enabling straightforward incorporation into peptide synthesis workflows. The electron-deficient thiazole ring enhances stability and facilitates selective derivatization under standard conditions.
(2-tert-Butoxycarbonylamino-thiazol-4-yl)-acetic acid serves as a versatile building block for thiazole-containing peptide mimetics and medicinal chemistry libraries. The tert-butyl carbamate group provides stable protection of the amine under standard reaction conditions, enabling selective deprotection during late-stage functionalization. The acetic acid moiety facilitates conjugation via ester or amide formation, while the thiazole ring offers structural rigidity and metabolic stability. This compound enables efficient access to bioactive scaffolds through established coupling protocols and is compatible with common purification methods.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: