CAS 499995-82-3
:Boc-(S)-3-Amino-3-(2,3-dichlorophenyl)-propionic acid
Description:
Boc-(S)-3-Amino-3-(2,3-dichlorophenyl)-propionic acid is a chemical compound characterized by its structure, which includes a Boc (tert-butyloxycarbonyl) protecting group attached to the amino group of an amino acid derivative. This compound features a chiral center, denoted by the (S) configuration, indicating its specific stereochemistry. The presence of a 2,3-dichlorophenyl group contributes to its unique properties, including potential biological activity and interactions. The Boc group serves as a protective moiety, facilitating the synthesis and manipulation of the amino acid in various chemical reactions, particularly in peptide synthesis. This compound is of interest in medicinal chemistry and drug development due to its potential applications in designing bioactive molecules. Its solubility, stability, and reactivity can vary based on the surrounding conditions, making it essential for researchers to consider these factors when utilizing this compound in experimental settings. Overall, Boc-(S)-3-Amino-3-(2,3-dichlorophenyl)-propionic acid exemplifies the complexity and utility of amino acid derivatives in chemical research.
Formula:C14H17Cl2NO4
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Boc-(s)-3-amino-3-(2,3-dichloro-phenyl)-propionic acid
CAS:Formula:C14H17Cl2NO4Purity:98%Color and Shape:SolidMolecular weight:334.1951(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,3-dichlorophenyl)propanoic acid
CAS:(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,3-dichlorophenyl)propanoic acidPurity:98%Molecular weight:334.2g/mol(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,3-dichlorophenyl)propanoic acid
CAS:Formula:C14H17Cl2NO4Purity:98%Molecular weight:334.19



