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Structure of 82834-12-6
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This chiral β-amino acid derivative features a stereodefined (S)-configuration at the C-2 position, combining a pendant ethoxy carbonyl group with a hydrophobic pentan-2-yl backbone. The molecule integrates a stable amide linkage and exhibits favorable solubility in organic solvents, enabling straightforward incorporation into peptide-based scaffolds under standard coupling conditions.
(S)-1-Ethoxy-1-oxopentan-2-yl-L-alanine serves as a versatile chiral building block for the synthesis of bioactive peptides and peptidomimetics. Its ethoxy-ketone functionality enables efficient α-alkylation and condensation reactions, while the protected L-alanine moiety provides stereocontrol and compatibility with standard peptide coupling protocols. Bench-stable and amenable to purification by flash chromatography, it facilitates the construction of complex heterocyclic scaffolds and medicinally relevant frameworks in iterative synthesis 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: