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Structure of 193537-14-3
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Ethyl 6-Boc-2-amino-4,7-dihydro-5H-thieno[2,3-c]pyridine-3-carboxylate features a protected amine and electron-rich heterocyclic core, enabling direct incorporation into complex scaffolds. The Boc group ensures stability during manipulations, while the thienopyridine framework supports diverse downstream transformations in medicinal chemistry and materials science.
Ethyl 6-Boc-2-amino-4,7-dihydro-5H-thieno[2,3-c]pyridine-3-carboxylate serves as a versatile building block for constructing thienopyridine-based heterocycles. The Boc-protected amine and ester functionalities enable sequential transformations, including deprotection, coupling reactions, and cyclization. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to medicinally relevant 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: