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Structure of 1035219-96-5
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2-Bromo-6,7-dihydrothiazolo[5,4-c]pyridin-4(5H)-one features a fused thiazolopyridinone core with a bromine substituent at the 2-position, enabling direct functionalization in late-stage diversification. The saturated five-membered ring enhances solubility and stability under standard conditions, while the carbonyl group supports hydrogen bonding in target engagement. This scaffold serves as a privileged motif in medicinal chemistry for kinase inhibition and protein-protein interaction modulation.
2-Bromo-6,7-dihydrothiazolo[5,4-c]pyridin-4(5H)-one serves as a versatile heterocyclic building block for medicinal chemistry and synthetic methodology development. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the thiazolopyridinone core provides a rigid, electron-deficient scaffold suitable for targeted functionalization. The compound exhibits good bench stability and facilitates efficient derivatization under standard reaction conditions.
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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: