Tert-butyl((1R,2R)-1-hydroxy-1-phenylhex-5-yn-2-yl)carbamate is a chemical compound characterized by its unique structure, which includes a tert-butyl group, a carbamate functional group, and a chiral center derived from a phenyl-substituted hex-5-yne. The presence of the hydroxy group contributes to its potential reactivity and solubility in polar solvents. This compound is likely to exhibit specific stereochemical properties due to its chiral centers, which can influence its biological activity and interactions with other molecules. The carbamate moiety suggests potential applications in medicinal chemistry, particularly in drug design, as carbamates are often used as prodrugs or in the synthesis of biologically active compounds. Additionally, the alkyne functionality may allow for further chemical modifications or reactions, such as click chemistry. Overall, this compound's characteristics make it of interest in various fields, including organic synthesis and pharmaceutical development.

tert-butyl((1R,2R)-1-hydroxy-1-phenylhex-5-yn-2-yl)carbamate

1437235-52-3: Tert-butyl((1R,2R)-1-hydroxy-1-phenylhex-5-yn-2-yl)carbamate is a chemical compound characterized by its unique structure, which includes a tert-butyl group, a carbamate functional group, and a chiral center derived from a phenyl-substituted hex-5-yne. The presence of the hydroxy group contributes to its potential reactivity and solubility in polar solvents. This compound is likely to exhibit specific stereochemical properties due to its chiral centers, which can influence its biological activity and interactions with other molecules. The carbamate moiety suggests potential applications in medicinal chemistry, particularly in drug design, as carbamates are often used as prodrugs or in the synthesis of biologically active compounds. Additionally, the alkyne functionality may allow for further chemical modifications or reactions, such as click chemistry. Overall, this compound's characteristics make it of interest in various fields, including organic synthesis and pharmaceutical development.

CAS 1437235-52-3

tert-butyl((1R,2R)-1-hydroxy-1-phenylhex-5-yn-2-yl)carbamate

Vibegron Impurity 7

Ref: ST-EA-CP-V23009