The chemical substance known as (2R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-5,5-dimethyl-2-pyrrolidinecarboxylic acid, with the CAS number 1310680-45-5, is a chiral compound featuring a pyrrolidine ring. This compound is characterized by the presence of a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis to protect amino groups. The dimethyl substitution on the pyrrolidine ring contributes to its steric properties, influencing its reactivity and interaction with biological systems. The carboxylic acid functional group provides acidic characteristics, allowing for potential interactions in various chemical environments. This compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its stereochemistry is crucial for biological activity, as the specific configuration can significantly affect the compound's binding affinity and efficacy in biological systems. Overall, this substance exemplifies the complexity and utility of chiral molecules in chemical research and applications.

(2R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-5,5-dimethyl-2-pyrrolidinecarboxylic acid

1310680-45-5: The chemical substance known as (2R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-5,5-dimethyl-2-pyrrolidinecarboxylic acid, with the CAS number 1310680-45-5, is a chiral compound featuring a pyrrolidine ring. This compound is characterized by the presence of a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis to protect amino groups. The dimethyl substitution on the pyrrolidine ring contributes to its steric properties, influencing its reactivity and interaction with biological systems. The carboxylic acid functional group provides acidic characteristics, allowing for potential interactions in various chemical environments. This compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its stereochemistry is crucial for biological activity, as the specific configuration can significantly affect the compound's binding affinity and efficacy in biological systems. Overall, this substance exemplifies the complexity and utility of chiral molecules in chemical research and applications.

(R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5,5-dimethylpyrrolidine-2-carboxylic acid

CAS 1310680-45-5

(2R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-5,5-dimethyl-2-pyrrolidinecarboxylic acid

(R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5,5-dimethylpyrrolidine-2-carboxylic acid

Ref: 54-OR1068381