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Structure of 668484-45-5
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This thiazole-based carboxylic acid features a tert-butyl-protected piperazine moiety, enabling straightforward deprotection and functionalization. The electron-deficient thiazole ring facilitates coupling reactions, while the pendant carboxylic acid supports conjugation in bioconjugation workflows. Designed for synthetic versatility in medicinal chemistry applications.
2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)thiazole-4-carboxylic acid serves as a versatile building block for medicinal chemistry, enabling the construction of thiazole-containing scaffolds via standard peptide coupling and Boc deprotection protocols. The piperazine moiety offers multiple sites for functionalization, while the carboxylic acid facilitates conjugation with amines or amine-containing intermediates. Its bench-stable nature and compatibility with common reaction conditions make it well-suited for iterative synthesis in API 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: