CAS 137102-30-8
:(S)-2-(Boc-amino)-2-phenylethylamine
Description:
(S)-2-(Boc-amino)-2-phenylethylamine is a chiral amine characterized by the presence of a Boc (tert-butyloxycarbonyl) protecting group on the amino functional group. This compound features a phenylethylamine backbone, which contributes to its potential biological activity. The Boc group is commonly used in organic synthesis to protect amines during various chemical reactions, allowing for selective functionalization of other reactive sites. The stereochemistry indicated by the (S) designation suggests that this compound has specific spatial arrangements that can influence its interaction with biological targets, making it of interest in medicinal chemistry and drug development. Additionally, the presence of both an amine and a phenyl group may enhance its solubility and reactivity, making it suitable for various synthetic applications. As with many chiral compounds, the enantiomeric purity can significantly affect its pharmacological properties, underscoring the importance of stereochemistry in the design of therapeutic agents.
Formula:C13H20N2O2
Synonyms:- Carbamic acid, [(1S)-2-amino-1-phenylethyl]-, 1,1-dimethylethyl ester
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Found 4 products.
(S)-tert-Butyl (2-amino-1-phenylethyl)carbamate
CAS:Formula:C13H20N2O2Purity:98%Color and Shape:SolidMolecular weight:236.3101(S)-2-(Boc-amino)-2-phenylethylamine
CAS:<p>(S)-2-(Boc-amino)-2-phenylethylamine</p>Purity:97%Color and Shape:SolidMolecular weight:236.31g/mol(S)-tert-Butyl (2-amino-1-phenylethyl)carbamate
CAS:Formula:C13H20N2O2Purity:95%Molecular weight:236.315tert-butyl N-[(1S)-2-amino-1-phenylethyl]carbamate
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H20N2O2Purity:Min. 95%Molecular weight:236.3 g/mol



