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Structure of 90989-12-1
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(S)-2-Aminohex-5-enoic acid features a chiral α-amino group paired with an isolated terminal alkene, enabling selective conjugate additions and facile derivatization. This scaffold integrates readily into peptidomimetics and bioactive oligomers, offering enhanced metabolic stability and conformational rigidity. The pendant double bond supports post-functionalization via hydrogenation or cycloaddition reactions.
(S)-2-Aminohex-5-enoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in peptide-based drug discovery. Its pendant enoic acid functionality enables conjugate additions and Michael-type reactions, while the α-amino and carboxylic acid groups support standard peptide coupling protocols. The (S)-configuration ensures stereochemical fidelity in target scaffolds, and the molecule exhibits good bench stability and ease of purification, making it well-suited for iterative synthetic workflows in medicinal chemistry.
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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: