The chemical substance known as (1S,3aR,6aS)-Hexahydrocyclopenta[c]pyrrole-1,2(1H)-dicarboxylic acid 2-(tert-butyl) ester, with CAS number 597569-42-1, is a complex organic compound characterized by its bicyclic structure, which includes a cyclopentane ring fused to a pyrrole moiety. This compound features two carboxylic acid functional groups, which are esterified with a tert-butyl group, enhancing its lipophilicity and potentially influencing its solubility and reactivity. The stereochemistry indicated by the (1S,3aR,6aS) configuration suggests specific spatial arrangements of atoms, which can significantly affect the compound's biological activity and interactions. Such compounds are often of interest in medicinal chemistry and drug development due to their potential pharmacological properties. The presence of multiple functional groups allows for various chemical modifications, making it a versatile scaffold for further synthetic exploration. Overall, this compound exemplifies the intricate relationship between molecular structure and chemical behavior, which is crucial in the fields of organic chemistry and pharmacology.

(1S,3aR,6aS)-Hexahydrocyclopenta[c]pyrrole-1,2(1H)-dicarboxylic acid 2-(tert-butyl) ester

597569-42-1: The chemical substance known as (1S,3aR,6aS)-Hexahydrocyclopenta[c]pyrrole-1,2(1H)-dicarboxylic acid 2-(tert-butyl) ester, with CAS number 597569-42-1, is a complex organic compound characterized by its bicyclic structure, which includes a cyclopentane ring fused to a pyrrole moiety. This compound features two carboxylic acid functional groups, which are esterified with a tert-butyl group, enhancing its lipophilicity and potentially influencing its solubility and reactivity. The stereochemistry indicated by the (1S,3aR,6aS) configuration suggests specific spatial arrangements of atoms, which can significantly affect the compound's biological activity and interactions. Such compounds are often of interest in medicinal chemistry and drug development due to their potential pharmacological properties. The presence of multiple functional groups allows for various chemical modifications, making it a versatile scaffold for further synthetic exploration. Overall, this compound exemplifies the intricate relationship between molecular structure and chemical behavior, which is crucial in the fields of organic chemistry and pharmacology.

HEXAHYDRO-CYCLOPENTA[C]PYRROLE-1,2-DICARBOXYLIC ACID 2-TERT-BUTYL ESTER

(1S,3aR,6aS)-2-(tert-Butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylic acid

CAS 597569-42-1

(1S,3aR,6aS)-Hexahydrocyclopenta[c]pyrrole-1,2(1H)-dicarboxylic acid 2-(tert-butyl) ester

HEXAHYDRO-CYCLOPENTA[C]PYRROLE-1,2-DICARBOXYLIC ACID 2-TERT-BUTYL ESTER

Ref: IN-DA00E9LM

(1S,3aR,6aS)-2-(tert-Butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylic acid

Ref: 54-OR1072313