1H-Pyrrole-1-acetic acid, α-(phenylmethyl)-, (S)-, with CAS number 46687-57-4, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing one nitrogen atom. This compound features an acetic acid moiety and a phenylmethyl group, contributing to its unique chemical properties. The (S)- designation indicates that it is a chiral molecule, specifically the S-enantiomer, which can exhibit different biological activities compared to its R counterpart. Typically, compounds like this may be involved in various chemical reactions, including those related to pharmaceuticals or agrochemicals, due to their ability to interact with biological systems. The presence of both the pyrrole and acetic acid functionalities suggests potential for hydrogen bonding and other intermolecular interactions, influencing solubility and reactivity. Overall, this compound's structure and stereochemistry play crucial roles in its chemical behavior and potential applications in medicinal chemistry or related fields.

1H-Pyrrole-1-acetic acid, a-(phenylmethyl)-, (S)-

46687-57-4: 1H-Pyrrole-1-acetic acid, α-(phenylmethyl)-, (S)-, with CAS number 46687-57-4, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing one nitrogen atom. This compound features an acetic acid moiety and a phenylmethyl group, contributing to its unique chemical properties. The (S)- designation indicates that it is a chiral molecule, specifically the S-enantiomer, which can exhibit different biological activities compared to its R counterpart. Typically, compounds like this may be involved in various chemical reactions, including those related to pharmaceuticals or agrochemicals, due to their ability to interact with biological systems. The presence of both the pyrrole and acetic acid functionalities suggests potential for hydrogen bonding and other intermolecular interactions, influencing solubility and reactivity. Overall, this compound's structure and stereochemistry play crucial roles in its chemical behavior and potential applications in medicinal chemistry or related fields.

CAS 46687-57-4

1H-Pyrrole-1-acetic acid, a-(phenylmethyl)-, (S)-

3-Phenyl-2-(1H-pyrrol-1-yl)propanoic acid

Ref: 3D-WBA68757