Indolizine, octahydro-, (R)-, with the CAS number 89772-92-9, is a bicyclic organic compound characterized by its unique structure, which consists of a fused indolizine ring system. This compound is a saturated derivative of indolizine, featuring a fully hydrogenated framework that contributes to its stability and reactivity. The (R)- designation indicates that it possesses a specific stereochemistry, which can influence its biological activity and interactions with other molecules. Indolizine derivatives are often studied for their potential applications in medicinal chemistry, particularly due to their ability to interact with biological targets. The compound may exhibit various physical properties, including solubility in organic solvents and specific melting and boiling points, which are typical for similar bicyclic structures. Additionally, its reactivity can be influenced by the presence of functional groups or substituents, making it a subject of interest in synthetic organic chemistry and drug development. Overall, the characteristics of Indolizine, octahydro-, (R)- highlight its significance in both theoretical and applied chemistry contexts.

Indolizine, octahydro-, (R)-

89772-92-9: Indolizine, octahydro-, (R)-, with the CAS number 89772-92-9, is a bicyclic organic compound characterized by its unique structure, which consists of a fused indolizine ring system. This compound is a saturated derivative of indolizine, featuring a fully hydrogenated framework that contributes to its stability and reactivity. The (R)- designation indicates that it possesses a specific stereochemistry, which can influence its biological activity and interactions with other molecules. Indolizine derivatives are often studied for their potential applications in medicinal chemistry, particularly due to their ability to interact with biological targets. The compound may exhibit various physical properties, including solubility in organic solvents and specific melting and boiling points, which are typical for similar bicyclic structures. Additionally, its reactivity can be influenced by the presence of functional groups or substituents, making it a subject of interest in synthetic organic chemistry and drug development. Overall, the characteristics of Indolizine, octahydro-, (R)- highlight its significance in both theoretical and applied chemistry contexts.

CAS 89772-92-9

Indolizine, octahydro-, (R)-

Indolizine, octahydro-, (R)-

Ref: IN-DA0040IG