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Structure of 463961-43-5
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3-(Bromomethyl)cyclobutanone features a reactive bromomethyl group attached to a cyclobutanone ring, enabling direct functionalization in synthetic transformations. This strained ketone derivative supports efficient carbon–carbon bond formation and serves as a key intermediate in the construction of cyclic scaffolds for medicinal chemistry and natural product synthesis.
3-(Bromomethyl)cyclobutanone serves as a versatile building block for constructing cyclobutane-containing scaffolds in medicinal chemistry and materials science. The bromomethyl group enables efficient functionalization via nucleophilic substitution, while the ketone moiety supports aldol condensations, enolate alkylations, and conjugate additions. Its bench-stable nature and compatibility with diverse reaction conditions facilitate straightforward incorporation into complex molecular architectures.
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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-H312-H332
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: