80651-74-7

Basic information

• Product Name: (2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one
• CAS NO: 80651-74-7
• Molecular Formula: C₂₇H₄₂O₇
• Molecular Weight: 478.6182
• Mol File: 80651-74-7.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 648.3°C at 760 mmHg
• Flash Point: 212.3°C
• Density: 1.31g/cm³
• Vapor Pressure: 1.51E-19mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: (2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one(80651-74-7)
• EPA Substance Registry System: (2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one(80651-74-7)

Safety Data

• Hazardous Substances Data: 80651-74-7(Hazardous Substances Data)

Usage

Description

(2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one is a complex sterol molecule derived from cholesterol, characterized by the presence of five hydroxyl groups, an epoxy group, and a ketone functional group. Its stereochemistry is defined by the specific configuration of the hydroxyl and chiral centers, denoted by Greek letter designations (beta and alpha). (2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one plays a significant role in various biological processes due to its unique structure and functional groups.

Uses

Used in Pharmaceutical Industry:
(2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one is used as a pharmaceutical agent for its potential therapeutic effects. The presence of multiple hydroxyl and epoxy groups allows for interactions with various biological targets, making it a candidate for the development of drugs targeting specific diseases or conditions.
Used in Research Applications:
This sterol molecule is utilized in research settings to study the structure-function relationships of sterols and their role in biological systems. Its unique configuration and functional groups provide valuable insights into the mechanisms of action and potential applications in various fields of research.
Used in Drug Delivery Systems:
(2beta,3beta,5beta,14xi,17alpha)-2,3,5,14,20-pentahydroxy-22,25-epoxycholest-7-en-6-one can be employed in the development of drug delivery systems, where its hydrophilic and hydrophobic properties can be leveraged to improve the solubility, stability, and bioavailability of therapeutic agents.