(S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate
$300.00
CAS No.: 1374635-44-5
Catalog No.: 193089
Purity: 95%
MF: C19H30N2O4
MW: 350.459
Storage: 2-8 degree Celsius
SMILES: CC([C@@H](CNC(OCC1=CC=CC=C1)=O)NC(OC(C)(C)C)=O)(C)C
Catalog No.: 193089
Purity: 95%
MF: C19H30N2O4
MW: 350.459
Storage: 2-8 degree Celsius
SMILES: CC([C@@H](CNC(OCC1=CC=CC=C1)=O)NC(OC(C)(C)C)=O)(C)C
(S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate; CAS No.: 1374635-44-5; (S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate. PROPERTIES: This compound appears as a white to off-white crystalline solid with molecular formula C16H25NO4 and a molecular weight of 283.38 g/mol. It exhibits a melting point in the range of 82-86 C and demonstrates 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 (S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate may cause skin irritation. The dicarbamate groups require careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, (S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its dimethyl substituents enable improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The dicarbamate-protected diamine group also facilitates controlled deprotection strategies in multi-step organic syntheses, as evidenced by methodological publications in synthetic chemistry.
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