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Structure of 197387-33-0
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4-(Bromomethyl)cyclohexan-1-one features a reactive bromomethyl group tethered to a cyclohexanone scaffold, enabling direct functionalization in synthetic transformations. This electrophilic handle facilitates efficient C–C bond formation via nucleophilic substitution, particularly in the construction of complex cyclic architectures. The molecule exhibits good stability under standard bench conditions and integrates readily into multi-step syntheses requiring selective alkylation.
4-(Bromomethyl)cyclohexan-1-one serves as a versatile synthetic building block for constructing functionalized cyclohexane scaffolds. The bromomethyl group enables efficient nucleophilic substitution reactions, while the ketone functionality supports enolization, aldol condensations, and reduction strategies. Its bench-stable nature and compatibility with diverse reaction conditions facilitate straightforward incorporation into complex molecular architectures, particularly in medicinal chemistry and natural product synthesis workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: