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*For research and further manufacturing use only, not for direct human use.
Structure of 2280-27-5
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(S)-2-Amino-3-hydroxy-3-methylbutanoic acid features a chiral center at the C2 position, delivering enantiomeric purity essential for asymmetric synthesis. The hydroxyl and methyl groups on the C3 carbon enhance solubility and steric control, enabling precise incorporation into peptide mimetics and bioactive scaffolds under standard bench conditions.
(S)-2-Amino-3-hydroxy-3-methylbutanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in peptidomimetic and β-amino alcohol scaffolds. Its hydroxyl and amino groups enable straightforward derivatization and orthogonal protection strategies, while the stereogenic center ensures high enantioselectivity in downstream transformations. Bench-stable and amenable to standard purification methods, it facilitates efficient access to complex heterocyclic motifs and medicinally relevant frameworks via established coupling and cyclization protocols.
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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: