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3β-(Benzoyloxy)-5α-cholest-8(14)-en-15-one is a complex organic compound with the molecular formula C33H48O3. It is a derivative of cholest-8(14)-en-15-one, a steroidal ketone, where a benzoyloxy group is attached to the 3β position. This chemical is characterized by its steroidal structure, which includes four fused rings and a side chain. The presence of the benzoyloxy group at the 3β position introduces an ester linkage, which can influence the compound's reactivity and solubility properties. 3β-(Benzoyloxy)-5α-cholest-8(14)-en-15-one is of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals or other steroidal derivatives due to its unique structural features.

7654-37-7

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7654-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7654-37-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7654-37:
(6*7)+(5*6)+(4*5)+(3*4)+(2*3)+(1*7)=117
117 % 10 = 7
So 7654-37-7 is a valid CAS Registry Number.

7654-37-7SDS

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 (3β,5α)-3-(benzoyloxy)cholest-8(14)-en-15-one

1.2 Other means of identification

Product number -
Other names 3β-benzoyloxy-5α-cholest-8(14)-en-15-one

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

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More Details:7654-37-7 SDS

7654-37-7Relevant academic research and scientific papers

Novel intermediates and an improved process for producing the compound (3β,5α)-3-hydroxycholest-8(14)-en-15-one

-

, (2008/06/13)

An improved process for the large scale production of the compound (3β,5α)-3-hydroxycholest-8(14)-en-15-one is described and two new compounds which have utility as intermediates in synthetic routes to the subject compound are disclosed.

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