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Structure of 149690-12-0
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This ethyl ester hydrochloride delivers a chiral, sterically defined scaffold featuring a biphenyl-4-yl moiety and a pendant amino group. Designed for synthetic accessibility, it integrates readily into peptide-like architectures and serves as a key intermediate in bioactive molecule development under standard conditions.
(2R,4S)-4-Amino-5-(biphenyl-4-yl)-2-methylpentanoic acid ethyl ester hydrochloride serves as a stereochemically defined chiral building block for the synthesis of bioactive molecules. The ethyl ester functionality enables straightforward derivatization, while the amino and carboxylic acid equivalents offer orthogonal handles for peptide coupling or heterocycle formation. Bench-stable and readily purified by standard chromatography, it functions effectively in solid-phase and solution-phase syntheses targeting pharmaceutically relevant scaffolds.
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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: