The chemical substance known as (E)7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-(3S,5S)-dihydroxyhept-6-enic acid ethyl ester, with the CAS number 380848-30-6, is a synthetic organic compound characterized by its complex structure, which includes a quinoline moiety, a cyclopropyl group, and a fluorophenyl substituent. This compound features a heptenoic acid backbone with dihydroxy functional groups, indicating potential for hydrogen bonding and reactivity. The presence of the ethyl ester group suggests that it may exhibit lipophilic properties, enhancing its solubility in organic solvents. The (E) configuration denotes a specific geometric arrangement around the double bond, which can influence the compound's biological activity and interactions. Such compounds are often investigated for their pharmacological properties, including potential applications in medicinal chemistry. Overall, the unique structural features of this compound may contribute to its reactivity and biological significance, making it a subject of interest in chemical and pharmaceutical research.

(E)7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-(3S,5S)-dihydroxyhept-6-enic acid ethyl ester

380848-30-6: The chemical substance known as (E)7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-(3S,5S)-dihydroxyhept-6-enic acid ethyl ester, with the CAS number 380848-30-6, is a synthetic organic compound characterized by its complex structure, which includes a quinoline moiety, a cyclopropyl group, and a fluorophenyl substituent. This compound features a heptenoic acid backbone with dihydroxy functional groups, indicating potential for hydrogen bonding and reactivity. The presence of the ethyl ester group suggests that it may exhibit lipophilic properties, enhancing its solubility in organic solvents. The (E) configuration denotes a specific geometric arrangement around the double bond, which can influence the compound's biological activity and interactions. Such compounds are often investigated for their pharmacological properties, including potential applications in medicinal chemistry. Overall, the unique structural features of this compound may contribute to its reactivity and biological significance, making it a subject of interest in chemical and pharmaceutical research.

CAS 380848-30-6

(E)7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-(3S,5S)-dihydroxyhept-6-enic acid ethyl ester

Pitavastatin (3S,5S)-Isomer Ethyl Ester

Ref: ST-EA-CP-P23022