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Structure of 19310-00-0
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(S)-2-Amino-3-(6-fluoro-1H-indol-3-yl)propanoic acid features a chiral center at the α-carbon, delivering enantiomerically pure access to fluorinated indole-containing peptides. The 6-fluoro substitution enhances electron-withdrawal and metabolic stability, while the carboxylic acid moiety enables direct incorporation into peptide backbones. This compound serves as a key building block for bioactive indole derivatives in medicinal chemistry.
(S)-2-Amino-3-(6-fluoro-1H-indol-3-yl)propanoic acid serves as a key chiral building block for indole-containing peptide analogs and bioactive scaffolds. The molecule combines a sterically defined (S)-α-amino acid backbone with a 6-fluoroindole moiety, enabling direct incorporation into peptidomimetics and CNS-targeted compounds. Its bench-stable crystalline form facilitates handling and purification, while the fluorinated indole enhances metabolic stability and modulates electronic properties for target engagement.
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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: