CAS 143615-00-3
:(2R,3S)-3-Phenylisoserine Ethylester
Description:
(2R,3S)-3-Phenylisoserine Ethylester is an organic compound characterized by its chiral centers, which contribute to its stereochemistry and potential biological activity. This compound features a phenyl group attached to the isoserine backbone, which is an amino acid derivative. The presence of the ethyl ester functional group enhances its lipophilicity, potentially influencing its solubility and permeability in biological systems. The specific stereochemistry, indicated by the (2R,3S) configuration, suggests that it may exhibit unique interactions with biological targets, such as enzymes or receptors, which could be relevant in medicinal chemistry. Additionally, the compound may participate in various chemical reactions typical of amino acids and esters, including hydrolysis and transesterification. Its structural characteristics may also allow for applications in the synthesis of peptides or as a building block in drug development. Overall, (2R,3S)-3-Phenylisoserine Ethylester represents a compound of interest in both synthetic and medicinal chemistry contexts.
- Ethyl(2R,3S)-3-(benzoylamino)-2-hydroxybenzenepropanoale
- (2R,3S)-3-Phenylisoserine ethyl ester
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Found 4 products.
Benzenepropanoic acid, b-amino-a-hydroxy-, ethyl ester, [R-(R*,S*)]-
CAS:Formula:C11H15NO3Purity:95%Color and Shape:SolidMolecular weight:209.2417Cabazitaxel Impurity 24 ( (2R,3S)-3-Amino-2-hydroxy-3-phenylpropionic Acid Ethyl Ester)
CAS:Formula:C11H15NO3Molecular weight:209.25(2R,3S)-3-Phenylisoserine Ethyl Ester
CAS:Controlled Product<p>Applications (2R,3S)-3-Phenylisoserine Ethyl Ester is a reactant used in the preparation of Taxotere and Taxol side chain.<br>References Forro, E. et al.: Tetrahedron: Assym., 21, 637 (2010); Commercon, A. et al.: Tetrahedron. Lett., 33, 5158 (1992)<br></p>Formula:C11H15NO3Color and Shape:NeatMolecular weight:209.24



