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2644-75-9

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2644-75-9 Usage

General Description

(3beta,5xi)-lanosta-7,9(11)-dien-3-ol is a chemical compound with the molecular formula C30H50O. It is a derivative of lanosterol, a common precursor in the biosynthesis of steroids. (3beta,5xi)-lanosta-7,9(11)-dien-3-ol is a triterpenoid alcohol, which means it is a member of a class of organic compounds derived from the precursor farnesyl pyrophosphate. It is commonly found in plants and can have various biological activities, including anti-inflammatory and anti-cancer properties. Additionally, it is also used in the production of certain pharmaceuticals and as a building block in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 2644-75-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2644-75:
(6*2)+(5*6)+(4*4)+(3*4)+(2*7)+(1*5)=89
89 % 10 = 9
So 2644-75-9 is a valid CAS Registry Number.

2644-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Dihydroagnosterol

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2644-75-9 SDS

2644-75-9Relevant articles and documents

First Demonstration of a Carbocation-Olefin Cyclization Route to the Lanosterol Series

Corey, E. J.,Lee, Jaemoon,Lin, David R.

, p. 9149 - 9152 (2007/10/02)

A silicon-assisted double carbocation-olefin cyclization reaction was used as the key step (10->11) in a simple, convergent and enatioselective total synthesis of lanostenol (1).

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