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Structure of 24599-25-5
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2-(Prop-2-enamido)acetic acid features a reactive enamide functionality paired with a carboxylic acid group, enabling direct conjugation in peptide synthesis and bioconjugation workflows. The α,β-unsaturated amide moiety facilitates Michael addition reactions under physiological conditions, while the pendant acid supports derivatization or salt formation for enhanced solubility. This bifunctional scaffold integrates readily into synthetic intermediates requiring both stability and site-specific reactivity.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P301+P330+P331-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: