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Structure of 21752-36-3
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This chiral benzoic acid derivative features a (S)-configured carbamoyl group attached to a phenylethyl moiety, enabling precise stereochemical control in asymmetric synthesis. The conjugated aromatic system enhances stability and facilitates integration into complex molecular architectures. Ideal for peptide mimetics and pharmaceutical intermediates requiring defined stereochemistry and enhanced solubility under standard conditions.
(S)-2-((1-Phenylethyl)carbamoyl)benzoic acid serves as a chiral building block for medicinal chemistry applications, enabling the synthesis of bioactive molecules through amide coupling and subsequent transformations. Its bench-stable structure features orthogonal functional groups—carboxylic acid and carbamoyl—that facilitate modular derivatization under standard conditions. The (S)-configuration provides stereochemical control in target-oriented synthesis, particularly relevant in peptidomimetic and heterocyclic scaffold construction.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: