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Structure of 52448-15-4
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(S)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid features a chiral center at the α-position, integrating a sterically defined indole scaffold with a chlorine substituent at the 5-position. This configuration enhances binding specificity in biological assays, while the carboxylic acid and amino functionalities enable direct incorporation into peptide sequences or conjugation workflows under standard conditions.
(S)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid serves as a key chiral building block for indole-containing peptide analogs and bioactive scaffolds. Its well-defined stereochemistry enables reliable incorporation into medicinal chemistry campaigns, while the 5-chloroindole moiety provides enhanced metabolic stability and favorable binding interactions. The molecule exhibits good bench stability, facilitates straightforward purification, and participates reliably in standard coupling reactions, making it a practical choice for targeted synthesis of complex heterocyclic compounds.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: