(R)-(2-amino-1-phenyl-ethyl)-carbamic acid benzyl ester
$225.00
CAS No.: 130406-35-8
Catalog No.: 193083
Purity: 95%
MF: C16H18N2O2
MW: 270.332
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)OC(N[C@@H](CN)C1=CC=CC=C1)=O
Catalog No.: 193083
Purity: 95%
MF: C16H18N2O2
MW: 270.332
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)OC(N[C@@H](CN)C1=CC=CC=C1)=O
(R)-(2-amino-1-phenyl-ethyl)-carbamic acid benzyl ester; CAS No.: 130406-35-8; (R)-(2-amino-1-phenyl-ethyl)-carbamic acid benzyl ester. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C15H16N2O2 and a molecular weight of 252.30 g/mol. It demonstrates a melting point in the range of 98-102 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as (R)-(2-amino-1-phenyl-ethyl)-carbamic acid benzyl ester may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, (R)-(2-amino-1-phenyl-ethyl)-carbamic acid benzyl ester serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on carbamate derivatives. Its amino group enables formation of bioactive amides through amidation reactions. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through formation of urea derivatives. Academic research has explored its potential in asymmetric catalysis for enantioselective synthesis, as reported in organic chemistry journals. The carbamate-protected amine group also facilitates controlled deprotection strategies in multi-step organic syntheses, as evidenced by methodological publications in synthetic chemistry.
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