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Structure of 788153-27-5
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(R)-3-Amino-3-(3-bromophenyl)propanoic acid features a chiral center flanked by an amino group and a para-brominated phenyl moiety, delivering high enantioselectivity in asymmetric synthesis. This bench-stable derivative integrates readily into peptidomimetic scaffolds and serves as a key intermediate for bioactive molecules requiring precise stereochemical control.
(R)-3-Amino-3-(3-bromophenyl)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide-based drug discovery. Its well-defined stereochemistry and compatibility with standard amine and carboxylic acid transformations enable reliable functionalization. The bromophenyl moiety provides a versatile handle for palladium-catalyzed cross-coupling reactions, facilitating the construction of complex aromatic scaffolds. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring high stereoselectivity and functional group integrity.
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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: