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Structure of 538368-15-9
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This chiral amino acid derivative features a stereodefined (2S) configuration at the alpha carbon, delivering precise control in peptide synthesis. The aminomethyl side chain enhances reactivity and solubility, enabling efficient incorporation into bioactive peptides and peptidomimetics under standard conditions.
(2S)-2-(Aminomethyl)butanoic acid serves as a chiral building block for peptidomimetics and bioactive molecule synthesis, offering a well-defined stereogenic center and a pendant primary amine. Its stability under standard reaction conditions facilitates straightforward functionalization, including amidation and alkylation, while the carboxylic acid group enables coupling reactions with minimal racemization. This structure functions effectively in solid-phase synthesis and supports the construction of complex heterocyclic scaffolds relevant to 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: