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Structure of 29262-58-6
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2-(Methylamino)-2-oxoacetic acid features a reactive carboxylate group paired with a methylamino substituent, enabling direct incorporation into peptide conjugation workflows. This bench-stable derivative facilitates site-specific labeling and bioconjugation under physiological conditions.
2-(Methylamino)-2-oxoacetic acid serves as a versatile building block for synthesizing β-amino carbonyl compounds and heterocyclic scaffolds. Its amide-like functionality enables reliable coupling reactions, while the α-amino ketone motif facilitates nucleophilic addition and condensation processes. The compound exhibits good bench stability and is readily purified by crystallization, making it suitable for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS07,GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H372-H411
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Precautionary Statements : P260-P264-P270-P273-P330-P391-P501
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Lot numbers can be found on the outside label of a product: