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Structure of 941-72-0
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4-Bromo-1-methylquinolin-2(1H)-one features a brominated quinolinone scaffold with enhanced electronic modulation from the methyl group at C1. This bench-stable, moisture-tolerant heterocycle integrates readily into transition-metal-catalyzed coupling reactions and serves as a key intermediate in medicinal chemistry for constructing complex nitrogen-containing frameworks.
4-Bromo-1-methylquinolin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The quinolinone core provides a rigid, planar scaffold with hydrogen-bonding capacity, facilitating interactions in target binding. Its methyl group enhances lipophilicity and metabolic stability, while the keto-enol tautomerism supports diverse derivatization pathways. Bench-stable and readily purified by crystallization, it functions effectively in modular synthesis of kinase inhibitors and other bioactive heterocycles.
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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: