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14546-23-7

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14546-23-7 Usage

General Description

(3beta)-N,N-dimethylcholest-5-en-3-amine, also known as dimethylcholest-5-en-3-amine, is a chemical compound with the molecular formula C29H51N. It is a derivative of cholesterol and belongs to the class of aminosteroids. (3beta)-N,N-dimethylcholest-5-en-3-amine is a tertiary amine, which means it contains three alkyl or aryl groups bonded to a nitrogen atom. Dimethylcholest-5-en-3-amine is used in the pharmaceutical industry for its potential medicinal properties, specifically as an intermediate in the synthesis of various steroids and other bioactive compounds. It may also have applications in research and development for understanding the biological functions of cholesterol and related molecules in the human body.

Check Digit Verification of cas no

The CAS Registry Mumber 14546-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14546-23:
(7*1)+(6*4)+(5*5)+(4*4)+(3*6)+(2*2)+(1*3)=97
97 % 10 = 7
So 14546-23-7 is a valid CAS Registry Number.

14546-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cholesterol propionate

1.2 Other means of identification

Product number -
Other names Cholesteryl-dimethyl-amin

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:14546-23-7 SDS

14546-23-7Relevant articles and documents

The dipolar aprotic-protic solution effects in the nucleophilic substitution of the cholesteryl tosylates

Bertho

, p. 155 - 173 (2007/10/06)

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