50932-24-6

Basic information

• Product Name: (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione
• Synonyms: ergosta-2,5,14,24-tetraene-1,26-dione, 22,26-epoxy-17,20-dihydroxy-, (22R)-
• CAS NO: 50932-24-6
• Molecular Formula: C₂₈H₃₆O₅
• Molecular Weight: 452.5824
• Mol File: 50932-24-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 643.8°C at 760 mmHg
• Flash Point: 213.4°C
• Density: 1.24g/cm³
• Vapor Pressure: 2.73E-19mmHg at 25°C
• Refractive Index: 1.605
• CAS DataBase Reference: (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione(50932-24-6)
• EPA Substance Registry System: (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione(50932-24-6)

Safety Data

• Hazardous Substances Data: 50932-24-6(Hazardous Substances Data)

Usage

Description

(22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione is a complex ergosterol derivative, a type of steroid compound, with a unique structure featuring multiple hydroxy and epoxy groups alongside a ketone group. (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione is derived from ergosterol, which is a precursor for vitamin D2 synthesis. Its intricate molecular architecture suggests a range of potential biological activities and applications in the pharmaceutical and medical fields, although further research is required to explore its full potential.

Uses

Used in Pharmaceutical Industry:
(22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione is used as a biologically active compound for its potential pharmacological activities. Given its complex structure with multiple functional groups, it may serve as a precursor for the synthesis of other medicinal compounds or be utilized directly for its inherent properties, which could include effects on cellular processes or interactions with specific biological targets.
Used in Medical Research:
In the medical research field, (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione is used as a subject of study to explore its potential applications in treating various conditions. Its unique structure may offer insights into new therapeutic approaches or provide a basis for developing novel drugs with specific mechanisms of action.
Used in Vitamin D2 Synthesis:
As a derivative of ergosterol, (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione plays a role in the synthesis of vitamin D2. This application is significant in the production of dietary supplements and in research aimed at understanding the role of vitamin D in human health and disease prevention.
Further research is necessary to fully understand the potential uses and effects of (22R)-17,20-dihydroxy-22,26-epoxyergosta-2,5,14,24-tetraene-1,26-dione, as its complex structure and biological activity suggest a wide range of possible applications in medicine and pharmaceuticals.