2867-93-8

Basic information

• Product Name: 3ALPHA,5-CYCLO-5ALPHA-CHOLESTAN-6BETA-OL METHYL ETHER
• Synonyms: 5-cyclo-5-alpha-cholestane,6-beta-methoxy-3-alph;6-beta-methoxy-3-alpha,5-cyclo-5-alpha-cholestane;6-methoxy-,(3-beta,5-alpha,6-beta)-5-cyclocholestane;6-methoxy-3,5-cyclocholestane;6-methoxy-5-cyclocholestane;I-CHOLESTEROL METHYL ETHER;I-CHOLESTERYL METHYL ETHER;6BETA-METHOXY-3ALPHA,5-CYCLOCHOLESTANE
• CAS NO: 2867-93-8
• Molecular Formula: C₂₈H₄₈O
• Molecular Weight: 400.68
• Mol File: 2867-93-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 436.2 °C at 760 mmHg
• Flash Point: 217.3 °C
• Appearance: /
• Density: 0.98 g/cm³
• Vapor Pressure: 2.11E-07mmHg at 25°C
• Refractive Index: 1.519
• Storage Temp.: −20°C
• CAS DataBase Reference: 3ALPHA,5-CYCLO-5ALPHA-CHOLESTAN-6BETA-OL METHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 3ALPHA,5-CYCLO-5ALPHA-CHOLESTAN-6BETA-OL METHYL ETHER(2867-93-8)
• EPA Substance Registry System: 3ALPHA,5-CYCLO-5ALPHA-CHOLESTAN-6BETA-OL METHYL ETHER(2867-93-8)

Safety Data

• WGK Germany: 3
• RTECS: GU2140000
• Hazardous Substances Data: 2867-93-8(Hazardous Substances Data)

Usage

General Description

3ALPHA,5-CYCLO-5ALPHA-CHOLESTAN-6BETA-OL METHYL ETHER, also known as 6-beta-methoxy-pregn-5-ene-3-beta-ol, is a synthetic chemical compound that belongs to the class of organic compounds known as cholanes and derivatives. It is a cholesterol derivative and is often used in research and chemical synthesis. 3ALPHA,5-CYCLO-5ALPHA-CHOLESTAN-6BETA-OL METHYL ETHER is a methyl ether of 3A,5-cyclo-5A-cholestan-6B-ol and has potential applications in pharmaceutical and chemical industries. Its unique structure and properties make it valuable in various applications, including as a reagent in organic synthesis and biochemistry research.

InChI:InChI=1/C28H48O/c1-18(2)8-7-9-19(3)22-10-11-23-21-16-25(29-6)28-17-20(28)12-15-27(28,5)24(21)13-14-26(22,23)4/h18-25H,7-17H2,1-6H3

Upstream product

• 2203-80-7 5-methylhex-1-yne 

Downstream Products

• 63469-10-3 S-cholesteryl-isothiourea; toluene-4-sulfonate 
• 481-21-0 cholestane 
• 1232680-84-0 3β-O-(1’,2’:3’,4’-di-O-isopropylidene-α-D-galactopyranos-6’-yl)cholest-5-ene 
• 1174-92-1 cholesteryl methyl ether 
• 57-88-5 cholesterol 
• 2469-23-0 dicholesteryl ether 
• 1981-90-4 (5α-cholestan-3β-yl)-methyl ether 
• 747-90-0 3,5-cholestadiene 
• 910-31-6 cholesteryl chloride 
• 6614-96-6 potassium cholesteryl sulphate 
• 809-51-8 7-ketocholesteryl acetate 
• 604-35-3 Cholesteryl acetate 
• 1255-86-3 O-isopropyl-cholesterol 
• 103325-29-7 ((3S,10R,13R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)(phenyl)sulfane 

Relevant articles and documents

STEREOCONTROLLED SYNTHESIS OF STEROID SIDE CHAIN; STEREOSELECTIVE SYNTHESES OF CHOLESTEROL AND 25-HYDROXYCHOLESTEROL

Novel stereoselective method to introduce side chain onto 17-oxosteroids has been deviced, and using the method cholesterol and 25-hydroxycholesterol are synthesized.