The chemical substance known as (3S,4R)-1-Boc-4-(3,4-Dimethoxyphenyl)Pyrrolidine-3-Carboxylic Acid, with the CAS number 959580-91-7, is a pyrrolidine derivative characterized by its specific stereochemistry and functional groups. The "Boc" (tert-butyloxycarbonyl) group serves as a protecting group for the amine, facilitating various synthetic applications. The presence of the 3,4-dimethoxyphenyl moiety contributes to its potential biological activity and solubility properties. This compound is typically utilized in organic synthesis, particularly in the development of pharmaceuticals, due to its structural features that may interact with biological targets. The stereochemistry indicated by the (3S,4R) configuration is crucial for its activity, as it can influence the compound's interaction with enzymes and receptors. Additionally, the carboxylic acid functional group can participate in various chemical reactions, such as esterification or amidation, further expanding its utility in synthetic chemistry. Overall, this compound exemplifies the complexity and versatility of organic molecules in medicinal chemistry.

(3S,4R)-1-Boc-4-(3,4-Dimethoxyphenyl)Pyrrolidine-3-Carboxylic Acid

959580-91-7: The chemical substance known as (3S,4R)-1-Boc-4-(3,4-Dimethoxyphenyl)Pyrrolidine-3-Carboxylic Acid, with the CAS number 959580-91-7, is a pyrrolidine derivative characterized by its specific stereochemistry and functional groups. The "Boc" (tert-butyloxycarbonyl) group serves as a protecting group for the amine, facilitating various synthetic applications. The presence of the 3,4-dimethoxyphenyl moiety contributes to its potential biological activity and solubility properties. This compound is typically utilized in organic synthesis, particularly in the development of pharmaceuticals, due to its structural features that may interact with biological targets. The stereochemistry indicated by the (3S,4R) configuration is crucial for its activity, as it can influence the compound's interaction with enzymes and receptors. Additionally, the carboxylic acid functional group can participate in various chemical reactions, such as esterification or amidation, further expanding its utility in synthetic chemistry. Overall, this compound exemplifies the complexity and versatility of organic molecules in medicinal chemistry.

CAS 959580-91-7

(3S,4R)-1-Boc-4-(3,4-Dimethoxyphenyl)Pyrrolidine-3-Carboxylic Acid

Boc-(+/-)-trans-4-(3,4-dimethoxy-phenyl)-pyrrolidine-3-carboxylic acid

Ref: IN-DA00IJN0