CAS 137102-65-9
:(R)-2-(Boc-amino)-2-phenylethylamine
Description:
(R)-2-(Boc-amino)-2-phenylethylamine, with the CAS number 137102-65-9, is a chiral amine that features a phenylethylamine backbone. The "Boc" in its name refers to the tert-butyloxycarbonyl group, which is a common protecting group for amines in organic synthesis. This compound is characterized by its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in the synthesis of pharmaceuticals and other organic compounds. The presence of the chiral center allows for the potential to produce enantiomerically pure products, which is crucial in medicinal chemistry due to the differing biological activities of enantiomers. Additionally, the compound is typically solid at room temperature and may exhibit solubility in organic solvents. Its stability and reactivity can be influenced by the presence of the Boc group, which can be removed under specific conditions to yield the free amine. Overall, (R)-2-(Boc-amino)-2-phenylethylamine is an important intermediate in the synthesis of biologically active molecules.
Formula:C13H20N2O2
Synonyms:- Carbamic acid, (2-amino-1-phenylethyl)-, 1,1-dimethylethyl ester, (R)-
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Found 4 products.
[(1R)-2-AMINO-1-PHENYLETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER
CAS:Formula:C13H20N2O2Purity:97%Color and Shape:SolidMolecular weight:236.3101(R)-2-(Boc-amino)-2-phenylethylamine
CAS:<p>(R)-2-(Boc-amino)-2-phenylethylamine</p>Purity:97%Molecular weight:236.31g/moltert-Butyl N-[(1R)-2-amino-1-phenylethyl]carbamate
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H20N2O2Purity:Min. 95%Molecular weight:236.31 g/mol



