(S)-N-BOC-2-amino-3-ethoxy-propionic acid, with the CAS number 104839-00-1, is a chiral amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino group. This compound features an ethoxy group attached to the propionic acid backbone, contributing to its unique properties. The BOC group is commonly used in peptide synthesis to protect the amino functionality, allowing for selective reactions at other sites. The presence of the ethoxy group enhances the hydrophobic character of the molecule, which can influence its solubility and reactivity in various solvents. As a chiral compound, it exists in two enantiomeric forms, with the (S)-configuration being biologically relevant in many contexts, particularly in pharmaceuticals and biochemistry. This compound is typically utilized in organic synthesis and research applications, especially in the development of peptide-based drugs and other bioactive molecules. Its stability and reactivity make it a valuable intermediate in synthetic chemistry.

(S)-N-BOC-2-AMINO-3-ETHOXY-PROPIONIC ACID

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(S)-N-Boc-2-amino-3-ethoxy-propionic acid

(S)-2-((tert-Butoxycarbonyl)amino)-3-ethoxypropanoic acid

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CAS 104839-00-1: (S)-N-BOC-2-AMINO-3-ETHOXY-PROPIONIC ACID

(S)-N-Boc-2-amino-3-ethoxy-propionic acid

Ref: 3D-EEA83900

(S)-N-BOC-2-AMINO-3-ETHOXY-PROPIONIC ACID

Ref: IN-DA0085K9

(S)-2-((tert-Butoxycarbonyl)amino)-3-ethoxypropanoic acid

Ref: 10-F634193

N-Boc-O-ethyl-L-serine, 97%

Ref: 02-H52781

(S)-N-Boc-2-amino-3-ethoxy-propionic acid

Ref: 54-OR307097