65377-86-8

Basic information

• Product Name: (3beta,5Z,7E,10alpha,22E)-9,10-Secoergosta-5,7,22-trien-3-ol
• Synonyms: (3beta,5Z,7E,10alpha,22E)-9,10-Secoergosta-5,7,22-trien-3-ol
• CAS NO: 65377-86-8
• Molecular Formula: C₂₈H₄₆O
• Molecular Weight: 398.66424
• Mol File: 65377-86-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 500℃
• Flash Point: 218℃
• Appearance: /
• Density: 1.003
• CAS DataBase Reference: (3beta,5Z,7E,10alpha,22E)-9,10-Secoergosta-5,7,22-trien-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3beta,5Z,7E,10alpha,22E)-9,10-Secoergosta-5,7,22-trien-3-ol(65377-86-8)
• EPA Substance Registry System: (3beta,5Z,7E,10alpha,22E)-9,10-Secoergosta-5,7,22-trien-3-ol(65377-86-8)

Safety Data

• Hazardous Substances Data: 65377-86-8(Hazardous Substances Data)

Usage

General Description

(3beta,5Z,7E,10alpha,22E)-9,10-Secoergosta-5,7,22-trien-3-ol, also known as Ergosterol, is a sterol compound found in fungi and yeast. It is a precursor of vitamin D2 and is important for the synthesis of cell membranes. Ergosterol has been studied for its potential health benefits, including its anti-inflammatory and antioxidant properties, as well as its role in promoting bone health. Additionally, it has been investigated for its potential use as a therapeutic agent for conditions such as cancer and infectious diseases. Ergosterol is commonly used as a supplement in the form of vitamin D2 to support overall health and wellness.

Upstream product

• 50-14-6 Calciferol 
• 57-87-4 Ergosterol 
• 67-56-1 methanol 
• 71-23-8 propan-1-ol 
• 64-17-5 ethanol 
• 56-23-5 tetrachloromethane 
• 107-21-1 ethylene glycol 
• 56-81-5 glycerol 
• 71-36-3 butan-1-ol 

Downstream Products

• 67-96-9 Dihydrotachysterol₂ 
• 104396-91-0 (7E,10S)-9,10-seco-ergosta-4,7,22t-trien-3-one 
• 104396-85-2 3.5-dinitro-benzoic acid-((3S:10S)-9.10-seco-ergostatrien-(5t.7c.22t)-yl-⁽³⁾-ester) 

Relevant articles and documents

Hydrotitanation-Protonation of Vitamin D2 and Its Analogues: An Efficient Method for the Preparation of 10,19-Dihydrovitamins D2 Including Dihydrotachysterol2

In this study we describe an easy and efficient method for the preparation of the known 10,19-dihydrovitamins D2 2b (DHV2-II), 2c (DHV2-IV), 3c (dihydrotachysterol2, DHT2), and the new dihydrovitamins D2 2f and 2g.This method is based on the regioselective hydrometalation reaction of vitamin D2 and its derivatives with the system Cp2TiCl2-LiAlH4 or Cp2TiCl2-Red-Al (Aldrich).Under optimal conditions, the reaction with the former of these hydrometalating systems takes place with a high degree of stereoselectivity and allows labelling at C-19.

Photochemical transformations. Part 34. Structures of the toxisterols.

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