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Structure of 16503-46-1
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2-Bromo-4-phenylbutanoic acid features a bromine-substituted aliphatic chain flanked by a phenyl group and a carboxylic acid, enabling direct functionalization in synthetic routes. This configuration supports efficient coupling reactions and facilitates incorporation into bioactive scaffolds requiring halogenated side chains.
2-Bromo-4-phenylbutanoic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenylalanine derivatives and bioactive heterocycles. Its α-brominated aliphatic chain facilitates nucleophilic substitution and elimination reactions under mild conditions. The molecule exhibits good bench stability, tolerates common functional groups, and simplifies purification via crystallization or standard chromatography. Functions effectively in coupling cascades and as a precursor for pharmaceutical intermediates requiring stereocontrolled side-chain elaboration.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: