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Structure of 222714-33-2
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(S)-4-(1-Aminoethyl)benzoic acid features a chiral α-amino acid scaffold with a para-substituted benzoic acid moiety, enabling integration into peptide-based pharmaceuticals and chemical probes. The stereogenic center ensures precise spatial orientation for targeted biological interactions, while the carboxylic acid group facilitates conjugation and salt formation. This bench-stable derivative supports synthetic applications requiring defined stereochemistry and functional handle availability.
(S)-4-(1-Aminoethyl)benzoic acid serves as a chiral building block for bioactive molecules, enabling the synthesis of pharmaceutically relevant arylalanine derivatives. Its well-defined stereochemistry and orthogonal functional groups facilitate straightforward derivatization via amidation, esterification, or coupling reactions. The compound exhibits good bench stability and is readily purified by crystallization, making it suitable for scalable synthesis in medicinal chemistry and process development workflows.
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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: