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Structure of 1092523-03-9
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6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one features a brominated tetrahydroquinoline core with a methyl group at nitrogen and a carbonyl at C2. This electron-deficient scaffold integrates readily into coupling reactions, offering high stability under standard conditions for medicinal chemistry applications.
6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one serves as a versatile building block for the synthesis of bioactive heterocycles, leveraging its bromine handle for palladium-catalyzed cross-coupling and the enamide functionality for further derivatization. The molecule exhibits bench stability, facilitates straightforward purification, and functions effectively in standard medicinal chemistry workflows involving Suzuki-Miyaura, Buchwald-Hartwig, or nucleophilic substitution reactions.
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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-H317-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P405-P501
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Lot numbers can be found on the outside label of a product: