Basic information

Product Name: (22E,24S)-27-Nor-5α-ergost-22-en-3β-ol
Synonyms: (22E,24S)-27-Nor-5α-ergost-22-en-3β-ol;Patinosterol
CAS NO:58514-32-2
Molecular Formula: C27H46O
Molecular Weight: 386.65
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 470.9°C at 760 mmHg
Flash Point: 206.5°C
Appearance: /
Density: 0.967g/cm³
Vapor Pressure: 7.58E-11mmHg at 25°C
Refractive Index: 1.514
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (22E,24S)-27-Nor-5α-ergost-22-en-3β-ol(CAS DataBase Reference)
NIST Chemistry Reference: (22E,24S)-27-Nor-5α-ergost-22-en-3β-ol(58514-32-2)
EPA Substance Registry System: (22E,24S)-27-Nor-5α-ergost-22-en-3β-ol(58514-32-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 58514-32-2(Hazardous Substances Data)

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58514-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58514-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58514-32:
(7*5)+(6*8)+(5*5)+(4*1)+(3*4)+(2*3)+(1*2)=132
132 % 10 = 2
So 58514-32-2 is a valid CAS Registry Number.

InChI:InChI=1/C27H46O/c1-6-18(2)7-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h7-8,18-25,28H,6,9-17H2,1-5H3/b8-7+/t18-,19+,20-,21-,22-,23+,24-,25-,26-,27+/m0/s1

58514-32-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name	(22E,24S)-27-nor-24-methyl-5α-cholest-22-en-3β-ol

1.2 Other means of identification

Product number	-
Other names	(3S,5S,8R,9S,10S,13R,14S,17R)-17-((E)-(1R,4S)-1,4-Dimethyl-hex-2-enyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58514-32-2 SDS

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58514-32-2Relevant academic research and scientific papers

Stereoselective Synthesis via Claisen Rearrangements of the Marine Sterols Occelasterol, Patinosterol, and 22,23-Dihydrooccelasterol

Hirano, Yutaka,Djerassi, Carl

, p. 2420 - 2426 (1982)

Occelasterol (1a), patinosterol (2a), 22,23-dihydrooccelasterol (3a), and their 24-stereoisomers (1b, 2b, and 3b) were stereoselectively synthesized.The i-methyl ether 6, derived from stigmasterol, was coupled with propynylmagnesium bromide to afford an e

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