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Structure of 365996-05-0
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tert-Butyl 2-amino-6,7-dihydrothiazolo[5,4-c]pyridine-5-(4H)-carboxylate features a fused thiazolopyridine core with a bench-stable tert-butyl ester and primary amine handle. This versatile scaffold integrates readily into medicinal chemistry campaigns, offering enhanced solubility and metabolic stability. The electron-rich heterocycle supports efficient coupling reactions and serves as a key intermediate in developing kinase inhibitors and bioactive small molecules.
tert-Butyl 2-amino-6,7-dihydrothiazolo[5,4-c]pyridine-5-(4H)-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and process development. The molecule combines a reducible thiazolopyridine core with a protected amine and ester functionality, enabling sequential transformations. Its bench-stable tert-butyl carbamate group facilitates selective deprotection, while the dihydrothiazole scaffold participates reliably in cross-coupling and cyclization reactions. Functions as a key intermediate in the synthesis of bioactive scaffolds requiring nitrogen-rich, fused heterocycles.
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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-H312-H315-H319-H332-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: