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Structure of 1078150-17-0
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2-Bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one features a fused thienopyridinone core with a bromine substituent at the 2-position, enabling direct functionalization in cross-coupling reactions. The saturated thiophene ring enhances solubility and stability under standard conditions, while the carbonyl group provides a key handle for derivatization. This scaffold serves as a privileged building block in medicinal chemistry.
2-Bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one serves as a versatile heterocyclic building block for medicinal chemistry and synthetic organic applications. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the lactam functionality provides structural rigidity and hydrogen-bonding capability. This scaffold exhibits good bench stability and compatibility with common protecting group strategies, facilitating efficient access to complex polycyclic systems through modular synthesis.
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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: