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Structure of 18928-94-4
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(2-Bromoethyl)cyclopentane features a bromoethyl chain tethered to a cyclopentane ring, delivering a reactive handle for nucleophilic substitution. This structure enables efficient coupling in synthetic transformations, particularly in the construction of functionalized cyclic systems under standard conditions.
(2-Bromoethyl)cyclopentane serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient functionalization of nucleophiles via SN2 displacement. Its cyclopentane backbone provides structural rigidity and enhanced metabolic stability, making it valuable for constructing bioactive scaffolds. The bromoethyl group exhibits high reactivity with thiols, amines, and enolates under mild conditions, facilitating rapid access to diverse heterocyclic systems and side-chain modifications. Bench-stable and readily purified by distillation or chromatography, it functions reliably in multistep synthesis workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: