CAS 31332-88-4
:benzyl (2-oxotetrahydrofuran-3-yl)carbamate
Description:
Benzyl (2-oxotetrahydrofuran-3-yl)carbamate is an organic compound characterized by its unique structure, which includes a tetrahydrofuran ring and a carbamate functional group. This compound typically exhibits a moderate to high polarity due to the presence of the carbamate moiety, which can engage in hydrogen bonding. Its molecular structure suggests potential applications in medicinal chemistry, particularly as a scaffold for drug development, owing to the tetrahydrofuran ring's ability to influence biological activity. The compound may also display moderate solubility in polar organic solvents, while its stability can be influenced by environmental factors such as pH and temperature. Additionally, the presence of the benzyl group may enhance lipophilicity, potentially affecting its pharmacokinetic properties. As with many organic compounds, safety data should be consulted to understand its toxicity and handling requirements. Overall, benzyl (2-oxotetrahydrofuran-3-yl)carbamate represents a versatile structure with potential applications in various chemical and pharmaceutical contexts.
Formula:C12H13NO4
InChI:InChI=1/C12H13NO4/c14-11-10(6-7-16-11)13-12(15)17-8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H,13,15)
SMILES:c1ccc(cc1)COC(=NC1CCOC1=O)O
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Found 3 products.
benzyl N-(2-oxotetrahydrofuran-3-yl)carbamate
CAS:Formula:C12H13NO4Purity:97%Molecular weight:235.2359Benzyl N-(2-oxooxolan-3-yl)carbamate
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13NO4Purity:Min. 95%Molecular weight:235.24 g/mol


