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Structure of 14469-83-1
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(5-Bromopentyl)benzene features a brominated aliphatic chain appended to a phenyl ring, enabling efficient coupling reactions in synthetic workflows. The benzylic bromide moiety serves as a reactive handle for nucleophilic substitution, facilitating the integration of aromatic scaffolds into complex molecular architectures under mild conditions. This compound offers reliable reactivity and bench-stable handling.
(5-Bromopentyl)benzene serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient functionalization of nucleophiles via SN2 displacement. Its benzylic bromide functionality offers high reactivity under mild conditions while maintaining bench stability and ease of purification. The flexible pentyl chain facilitates incorporation into diverse molecular architectures, including heterocyclic scaffolds and macrocyclic systems, making it a practical building block for 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 : 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: