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Pregn-5-en-3-ol,20-methyl-21-[(3R)-3- methyl-2-(1-methylethyl)-1-cyclopropen-1- yl]-,(3â,20R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57331-04-1

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57331-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57331-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,3 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57331-04:
(7*5)+(6*7)+(5*3)+(4*3)+(3*1)+(2*0)+(1*4)=111
111 % 10 = 1
So 57331-04-1 is a valid CAS Registry Number.

57331-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name calysterol

1.2 Other means of identification

Product number -
Other names (3S,8S,9S,10R,13R,14S)-17-[(R)-2-((R)-2-Isopropyl-3-methyl-cycloprop-1-enyl)-1-methyl-ethyl]-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:57331-04-1 SDS

57331-04-1Relevant articles and documents

ACID-CATALYZED AND PHOTOCHEMICAL ISOMERIZATION OF STEROIDAL CYCLOPROPENES.

Itoh,Djerssi

, p. 4407 - 4416 (1983)

The acid-catalyzed and photochemical isomerization of two naturally occurring steroidal cyclopropenes, (28R)-calysterol and (23R)-23H-isocalysterol is described. Cyclopropene on treatment with methanolic sulfuric acid afforded 23-ethylated cholesterol derivatives containing conjugated diene systems or methoxylated side chains. The sole production of C-23 ethylated sterols demonstrates that this cyclopropene undergoes acid-promoted bond cleavage only between C-24 and C-28. By contrast, methanolic sulfuric acid treatment of the isomeric cyclopropene generated conjugated dienes with 24-methyl-24-homocholestane and 24-ethylcholestane side chains, together with their methoxylated derivatives. This implies that bond fission between C-23 and C-24, as well as C-23 and C-28, is operating in this instance, which is of mechanistic significance.

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