Methyl [(1R)-2-hydroxy-1,2,2-triphenylethyl]carbamate, identified by its CAS number 352535-67-2, is a chemical compound characterized by its carbamate functional group, which is derived from the reaction of a carbamic acid with an alcohol. This compound features a triphenylethyl moiety, indicating the presence of three phenyl groups attached to a central carbon, contributing to its significant steric bulk and potential for unique interactions in biological systems. The hydroxyl group in the structure suggests the potential for hydrogen bonding, which can influence its solubility and reactivity. Methyl [(1R)-2-hydroxy-1,2,2-triphenylethyl]carbamate may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its stereochemistry, indicated by the (1R) configuration, suggests that it may have specific interactions with biological targets, which can be crucial for its activity. Overall, this compound's unique structural features may lead to diverse applications in research and industry, particularly in the development of pharmaceuticals or agrochemicals.

methyl [(1R)-2-hydroxy-1,2,2-triphenylethyl]carbamate

352535-67-2: Methyl [(1R)-2-hydroxy-1,2,2-triphenylethyl]carbamate, identified by its CAS number 352535-67-2, is a chemical compound characterized by its carbamate functional group, which is derived from the reaction of a carbamic acid with an alcohol. This compound features a triphenylethyl moiety, indicating the presence of three phenyl groups attached to a central carbon, contributing to its significant steric bulk and potential for unique interactions in biological systems. The hydroxyl group in the structure suggests the potential for hydrogen bonding, which can influence its solubility and reactivity. Methyl [(1R)-2-hydroxy-1,2,2-triphenylethyl]carbamate may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its stereochemistry, indicated by the (1R) configuration, suggests that it may have specific interactions with biological targets, which can be crucial for its activity. Overall, this compound's unique structural features may lead to diverse applications in research and industry, particularly in the development of pharmaceuticals or agrochemicals.

(R)-(+)-N-Carbomethoxy-2-amino-1,1,2-triphenylethanol

<p>(R)-(+)-N-Carbomethoxy-2-amino-1,1,2-triphenylethanol</p>

CAS 352535-67-2

methyl [(1R)-2-hydroxy-1,2,2-triphenylethyl]carbamate

(R)-(+)-N-Carbomethoxy-2-amino-1,1,2-triphenylethanol

Ref: IN-DA003C66

(R)-(+)-N-Carbomethoxy-2-amino-1,1,2-triphenylethanol

Ref: 54-OR304027