benzyl but-3-yn-2-ylcarbamate
$225.00
CAS No.: 1393576-61-8
Catalog No.: 193094
Purity: 95%
MF: C12H13NO2
MW: 203.241
Storage: 2-8 degree Celsius
SMILES: CC(C#C)NC(OCC1=CC=CC=C1)=O
Catalog No.: 193094
Purity: 95%
MF: C12H13NO2
MW: 203.241
Storage: 2-8 degree Celsius
SMILES: CC(C#C)NC(OCC1=CC=CC=C1)=O
benzyl but-3-yn-2-ylcarbamate; CAS No.: 1393576-61-8; benzyl but-3-yn-2-ylcarbamate. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C12H13NO2 and a molecular weight of 203.24 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 benzyl but-3-yn-2-ylcarbamate may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, benzyl but-3-yn-2-ylcarbamate serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on carbamate derivatives. Its alkyne substituent enables participation in click chemistry reactions for constructing complex molecules. 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 bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical 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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