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Structure of 3279-90-1
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6-Bromo-1,2,3,4-tetrahydro-2-quinolinone features a brominated quinolinone core with enhanced reactivity at the C6 position. This bench-stable heterocycle integrates readily into cross-coupling reactions and serves as a key scaffold for medicinal chemistry libraries. The electron-deficient ring system pairs effectively with palladium catalysts, enabling efficient functionalization under mild conditions.
6-Bromo-1,2,3,4-tetrahydro-2-quinolinone serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted quinoline scaffolds via palladium-catalyzed cross-coupling reactions. Its bromine substituent offers high reactivity in Suzuki, Stille, and Negishi couplings, while the tetrahydroquinolinone core provides a stable, functionalized platform for further derivatization. The compound exhibits excellent bench stability and compatibility with common protecting group strategies, facilitating straightforward purification and integration into multi-step syntheses.
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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: