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3β-acetoxy-5α-stigmastane is a naturally occurring steroid compound, belonging to the stigmastane family of steroids. It is characterized by a 3β-acetoxy group and a 5α-configuration, which refers to the position of the hydroxyl group and the double bond in the molecule. 3β-acetoxy-5α-stigmastane is derived from plant sterols and is found in various plant oils, such as soybean oil and corn oil. It plays a role in the biosynthesis of other steroids and has potential applications in the pharmaceutical and chemical industries. The structure of 3β-acetoxy-5α-stigmastane is crucial for understanding its properties and potential uses, making it an important compound in the field of organic chemistry.

2364-21-8

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2364-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2364-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2364-21:
(6*2)+(5*3)+(4*6)+(3*4)+(2*2)+(1*1)=68
68 % 10 = 8
So 2364-21-8 is a valid CAS Registry Number.

2364-21-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names 5alpha-Sitostan-3beta-ol acetate

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:2364-21-8 SDS

2364-21-8Relevant academic research and scientific papers

Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters. Part I. Regioselective hydrogenation of stigmasterol: An easy access to oxyphytosterols

Geoffroy, Philippe,Julien-David, Diane,Marchioni, Eric,Raul, Francis,Aoude-Werner, Dalal,Miesch, Michel

, p. 702 - 707 (2008)

The synthesis of several oxyphytosterols is described starting from stigmasterol, the key step being the regioselective hydrogenation of the 22-23 double bond of the latter.

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