Carbamic acid, bis(phenylmethyl) ester, with the specified structure, is a complex organic compound characterized by its carbamate functional group. This compound features a pyrrolidine ring and a butanediyl chain, which contribute to its unique chemical properties. The presence of two phenylmethyl ester groups enhances its lipophilicity, potentially influencing its solubility and reactivity in organic solvents. The stereochemistry indicated by the (S) designation suggests that the compound exhibits chirality, which may affect its biological activity and interactions with other molecules. As a carbamate derivative, it may participate in reactions typical of carbamates, such as hydrolysis or transesterification. The compound's potential applications could span various fields, including pharmaceuticals and agrochemicals, where carbamate structures are often utilized for their biological activity. However, specific safety and handling guidelines should be followed due to the potential toxicity associated with carbamate compounds. Overall, this compound exemplifies the complexity and versatility of organic chemistry in synthesizing molecules with specific functional groups and structural features.

Carbamic acid,[1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-1,4-butanediyl]bis-,bis(phenylmethyl) ester, (S)- (9CI)

90970-61-9: Carbamic acid, bis(phenylmethyl) ester, with the specified structure, is a complex organic compound characterized by its carbamate functional group. This compound features a pyrrolidine ring and a butanediyl chain, which contribute to its unique chemical properties. The presence of two phenylmethyl ester groups enhances its lipophilicity, potentially influencing its solubility and reactivity in organic solvents. The stereochemistry indicated by the (S) designation suggests that the compound exhibits chirality, which may affect its biological activity and interactions with other molecules. As a carbamate derivative, it may participate in reactions typical of carbamates, such as hydrolysis or transesterification. The compound's potential applications could span various fields, including pharmaceuticals and agrochemicals, where carbamate structures are often utilized for their biological activity. However, specific safety and handling guidelines should be followed due to the potential toxicity associated with carbamate compounds. Overall, this compound exemplifies the complexity and versatility of organic chemistry in synthesizing molecules with specific functional groups and structural features.

CAS 90970-61-9

Carbamic acid,[1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-1,4-butanediyl]bis-,bis(phenylmethyl) ester, (S)- (9CI)