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Structure of 888491-84-7
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This bromomethyl ether features a reactive alkylating handle for conjugation workflows. The benzylic bromide moiety enables efficient coupling with nucleophiles under mild conditions, while the ether linkage provides stability and solubility in common organic solvents. Ideal for building molecular architectures in synthetic and medicinal chemistry applications.
((2-Bromopropoxy)methyl)benzene serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient introduction of propoxy-containing moieties under mild conditions. Its bromine functionality facilitates nucleophilic substitution reactions with amines, thiols, and carbanions, while the benzylic position enhances reactivity without compromising bench stability. The molecule exhibits good functional group tolerance and is compatible with standard purification methods, making it ideal for building complex intermediates in medicinal chemistry and materials science applications.
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Lot numbers can be found on the outside label of a product: