(9S)-9-(Phenylmethoxy)-Cinchonan-6'-ol, identified by the CAS number 761434-35-9, is a chemical compound that belongs to the class of cinchona alkaloids, which are derived from the bark of the cinchona tree. This compound features a cinchona backbone, characterized by a bicyclic structure that includes a quinoline and a quinuclidine moiety. The presence of a phenylmethoxy group at the 9-position contributes to its unique properties, potentially influencing its solubility and reactivity. The hydroxyl group at the 6' position can participate in hydrogen bonding, which may enhance its biological activity. Compounds of this class are often studied for their pharmacological properties, including their potential as chiral catalysts or in medicinal chemistry for their antimalarial and analgesic effects. The stereochemistry indicated by the (9S) configuration suggests specific spatial arrangements that can significantly affect the compound's interactions with biological targets. Overall, (9S)-9-(phenylmethoxy)-Cinchonan-6'-ol represents a structurally interesting compound with potential applications in various fields of chemistry and pharmacology.

(9S)- 9-(phenylMethoxy)-Cinchonan-6'-ol

761434-35-9: (9S)-9-(Phenylmethoxy)-Cinchonan-6'-ol, identified by the CAS number 761434-35-9, is a chemical compound that belongs to the class of cinchona alkaloids, which are derived from the bark of the cinchona tree. This compound features a cinchona backbone, characterized by a bicyclic structure that includes a quinoline and a quinuclidine moiety. The presence of a phenylmethoxy group at the 9-position contributes to its unique properties, potentially influencing its solubility and reactivity. The hydroxyl group at the 6' position can participate in hydrogen bonding, which may enhance its biological activity. Compounds of this class are often studied for their pharmacological properties, including their potential as chiral catalysts or in medicinal chemistry for their antimalarial and analgesic effects. The stereochemistry indicated by the (9S) configuration suggests specific spatial arrangements that can significantly affect the compound's interactions with biological targets. Overall, (9S)-9-(phenylmethoxy)-Cinchonan-6'-ol represents a structurally interesting compound with potential applications in various fields of chemistry and pharmacology.

CAS 761434-35-9

(9S)- 9-(phenylMethoxy)-Cinchonan-6'-ol

4-((1S)-(Benzyloxy)((1S,2R,5R)-5-vinylquinuclidin-2-yl)methyl)quinolin-6-ol

Ref: IN-DA00GHWU