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Structure of 75266-38-5
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(S)-2-Aminobut-3-enoic acid hydrochloride features a chiral α-amino acid scaffold with a conjugated enoic acid moiety, enabling direct incorporation into peptide architectures. The hydrochloride salt enhances solubility and stability under standard handling conditions, facilitating use in synthetic peptide coupling reactions and bioactive molecule design.
(S)-2-Aminobut-3-enoic acid hydrochloride serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in peptide-based drug discovery. Its conjugated enamine–acid functionality enables efficient coupling reactions and participates reliably in Michael additions and cyclization cascades. The hydrochloride salt enhances stability and solubility, facilitating handling and purification in standard synthetic 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: