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Structure of 165947-52-4
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tert-Butyl 4,5-dihydrothieno[2,3-c]pyridine-6(7H)-carboxylate features a fused thienopyridine core with a reducible lactam-like carbonyl functionality. This bench-stable scaffold integrates seamlessly into synthetic routes requiring electron-rich heterocycles, enabling efficient access to bioactive analogs in medicinal chemistry campaigns.
tert-Butyl 4,5-dihydrothieno[2,3-c]pyridine-6(7H)-carboxylate serves as a versatile scaffold for constructing biologically relevant heterocycles, enabling direct functionalization at the 6-position via standard deprotonation or electrophilic substitution. The dihydrothienopyridine core exhibits robust bench stability and compatibility with diverse coupling reactions, while the tert-butyl ester facilitates straightforward hydrolysis or further derivatization under mild conditions. Functions effectively in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
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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: