The chemical substance known as (3R,5Z,7E,17xi)-24,24-difluoro-9,10-secocholesta-5,7,10-triene-3,25-diol, with the CAS number 71603-41-3, is a complex organic compound characterized by its unique structural features. It belongs to the class of steroids, specifically a seco-steroid, which indicates that it has undergone a cleavage in the steroid framework. The presence of difluoro substituents suggests enhanced reactivity and potential biological activity, as fluorine atoms can significantly influence the compound's lipophilicity and metabolic stability. The configuration of the double bonds (5Z, 7E) and the stereochemistry at the 3-position (3R) contribute to its specific three-dimensional shape, which is crucial for interactions with biological targets. Additionally, the presence of hydroxyl groups (diol) indicates potential for hydrogen bonding, which may enhance solubility in polar solvents. Overall, this compound's unique structural and functional characteristics make it of interest in medicinal chemistry and biochemistry, particularly in the study of steroidal compounds and their derivatives.

(3R,5Z,7E,17xi)-24,24-difluoro-9,10-secocholesta-5,7,10-triene-3,25-diol

71603-41-3: The chemical substance known as (3R,5Z,7E,17xi)-24,24-difluoro-9,10-secocholesta-5,7,10-triene-3,25-diol, with the CAS number 71603-41-3, is a complex organic compound characterized by its unique structural features. It belongs to the class of steroids, specifically a seco-steroid, which indicates that it has undergone a cleavage in the steroid framework. The presence of difluoro substituents suggests enhanced reactivity and potential biological activity, as fluorine atoms can significantly influence the compound's lipophilicity and metabolic stability. The configuration of the double bonds (5Z, 7E) and the stereochemistry at the 3-position (3R) contribute to its specific three-dimensional shape, which is crucial for interactions with biological targets. Additionally, the presence of hydroxyl groups (diol) indicates potential for hydrogen bonding, which may enhance solubility in polar solvents. Overall, this compound's unique structural and functional characteristics make it of interest in medicinal chemistry and biochemistry, particularly in the study of steroidal compounds and their derivatives.

CAS 71603-41-3

(3R,5Z,7E,17xi)-24,24-difluoro-9,10-secocholesta-5,7,10-triene-3,25-diol