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Structure of 40299-87-4
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2-Bromo-1-(morpholin-4-yl)ethanone features a bromine-substituted acetyl group linked to a morpholine ring, delivering a potent electrophilic handle for nucleophilic substitution. This bench-stable ketone integrates readily into synthetic sequences requiring controlled C–C or C–heteroatom bond formation, particularly in medicinal chemistry and heterocycle synthesis.
2-Bromo-1-(morpholin-4-yl)ethanone serves as a versatile acylating agent in synthetic organic chemistry, enabling the introduction of morpholine-containing acyl groups under mild conditions. Its bromo substituent facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions, while the morpholinyl moiety offers favorable solubility and functional group tolerance. This reagent functions effectively in the construction of heterocyclic scaffolds and peptide analogs, with bench-stable handling and straightforward purification by chromatography or crystallization.
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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: