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Structure of 3814-32-2
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Bromomethylcycloheptane serves as a versatile alkylating agent featuring a reactive bromomethyl group tethered to a cycloheptane ring. This configuration enables efficient functionalization in synthetic routes requiring bulky, ring-strained electrophiles. The molecule exhibits favorable stability under standard conditions and integrates readily into complex molecular architectures through nucleophilic substitution processes.
(Bromomethyl)cycloheptane serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient functionalization of nucleophiles via SN2 displacement. Its cycloheptane framework provides enhanced stability and solubility compared to smaller cyclic analogs, while the primary bromide functionality ensures high reactivity under mild conditions. The compound exhibits excellent functional group tolerance and facilitates clean transformations, making it well-suited for building complex scaffolds in medicinal chemistry and materials science applications.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: