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The chemical compound "5α(H),17α(H)-(20R)-3β-acetoxycholest-8(14)-ene" is a steroid derivative, specifically a cholestane with a double bond between carbons 8 and 14. It features a 3β-acetoxy group, indicating an acetate ester at the 3β position, and a hydroxyl group at both the 5α and 17α positions. 5ALPHA(H),17ALPHA(H)-(20R)-3BETA-ACETOXYCHOLEST-8(14)-ENE is characterized by its unique stereochemistry, with the 20R configuration referring to the chiral center at carbon 20. It is a complex molecule with a specific arrangement of functional groups that can be found in various biological contexts, such as in the synthesis of certain hormones or as an intermediate in the production of pharmaceuticals. The compound's structure and properties make it a subject of interest in organic chemistry and biochemistry.

6562-21-6

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6562-21-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6562-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6562-21:
(6*6)+(5*5)+(4*6)+(3*2)+(2*2)+(1*1)=96
96 % 10 = 6
So 6562-21-6 is a valid CAS Registry Number.

6562-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5ALPHA(H),17ALPHA(H)-(20R)-3BETA-ACETOXYCHOLEST-8(14)-ENE

1.2 Other means of identification

Product number -
Other names 2'-Aminothiazol<5',4':2,3>-2-cholesten

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:6562-21-6 SDS

6562-21-6Relevant academic research and scientific papers

Inhibitors of sterol synthesis. Synthesis and spectral properties of 3β-hydroxy-5α-cholestan-15-one and its 14β-epimer and their effects on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity

Siddiqui,Wilson,Parish,Gerst,Pinkerton,Schroepfer Jr.

, p. 1 - 15 (2007/10/02)

3β-Hydroxy-5α-cholestan-15-one (2a) and its 14β-epimer 2b were prepared from 3β-acetoxy-5α-cholest-8(14)-ene (3). Hydroboration of 3 at 45-50°C gave a mixture of 5α,14α-cholestane-3β,15α-diol and 5α,14β-cholestane-3β,15β-diol, which were separated on sili

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