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3β-acetoxy-27-norcholest-5-en-25-one is a complex organic compound belonging to the steroid family, characterized by its unique molecular structure. 3β-acetoxy-27-norcholest-5-en-25-one features a cholestane-based skeleton, with a double bond at the 5th position and a ketone group at the 25th position. The 3β position is occupied by an acetoxy group, which is an acetate ester of a hydroxyl group, while the 27th position is missing a carbon atom, making it a norcholestane derivative. This specific arrangement of functional groups and atoms contributes to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals and chemical research.

7548-94-9

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7548-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7548-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7548-94:
(6*7)+(5*5)+(4*4)+(3*8)+(2*9)+(1*4)=129
129 % 10 = 9
So 7548-94-9 is a valid CAS Registry Number.

7548-94-9SDS

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

1.2 Other means of identification

Product number -
Other names -

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

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More Details:7548-94-9 SDS

7548-94-9Upstream product

7548-94-9Relevant academic research and scientific papers

Preparation of 3β-hydroxy-27-norcholest-5-ene-25-one and intermediates thereof

-

, (2008/06/13)

A process for preparing 3β-hydroxy-27-norcholest-5-ene-25-one, a useful intermediate in the synthesis of 25-acetoxy vitamin D3, novel intermediates, and preparation thereof are disclosed.

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