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55870-01-4

(3beta,28S)-24,28-epoxystigmast-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55870-01-4

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55870-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55870-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,7 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55870-01:
(7*5)+(6*5)+(5*8)+(4*7)+(3*0)+(2*0)+(1*1)=134
134 % 10 = 4
So 55870-01-4 is a valid CAS Registry Number.

55870-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (24S,28S)-24,28-epoxystigmast-5-en-3β-ol

1.2 Other means of identification

Product number -
Other names (3S,8S,9S,10R,13R,14S,17R)-17-[(R)-3-((2S,3S)-2-Isopropyl-3-methyl-oxiranyl)-1-methyl-propyl]-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-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:55870-01-4 SDS

55870-01-4Relevant articles and documents

Substrate Stereospecificity in the Metabolism of Fucosterol and Isofucosterol 24,28-Epoxides in Tenebrio molitor

Nicotra, Francesco,Pizzi, Patrizia,Ronchetti, Fiamma,Russo, Giovanni,Toma, Lucio

, p. 480 - 483 (1981)

It is shown that the insect Tenebrio molitor is able to convert the (24R,28S)-isofucosterol epoxide into cholesterol much better than the (24S,28R)-isomer; on the other hand, the (24R,28R)- and the (24S,28S)-fucosterol epoxides are transformed into cholesterol at about the same extent.

Synthesis of (24R,28R)- and (24S,28S)-Fucosterol Epoxides. Revision of C-24,28 Configurations

Fujimoto, Yoshinori,Murakami, Kazuo,Ikekawa, Nobuo

, p. 566 - 569 (2007/10/02)

A facile synthesis of (24R,28R)- and (24S,28S)-24,28-epoxyfucosterol from fucosterol via the 24,28-glycols is described.The C-24,28 configurations were established by chemical correlation with sitosterol and clionasterol and show that previous assignments

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