2644-75-9 Usage
Description
(3beta,5xi)-lanosta-7,9(11)-dien-3-ol, a chemical compound with the molecular formula C30H50O, is a triterpenoid alcohol derived from lanosterol, a common precursor in the biosynthesis of steroids. As a member of the class of organic compounds derived from farnesyl pyrophosphate, it is commonly found in plants and exhibits various biological activities, such as anti-inflammatory and anti-cancer properties.
Uses
Used in Pharmaceutical Industry:
(3beta,5xi)-lanosta-7,9(11)-dien-3-ol is used as a building block for the production of certain pharmaceuticals, leveraging its versatile chemical structure and biological activities.
Used in Organic Synthesis:
This triterpenoid alcohol is also utilized as a key component in organic synthesis, allowing for the creation of various complex molecules and compounds.
Used in Anti-inflammatory Applications:
(3beta,5xi)-lanosta-7,9(11)-dien-3-ol is employed for its anti-inflammatory properties, potentially offering therapeutic benefits in the treatment of inflammation-related conditions.
Used in Anti-cancer Applications:
Due to its anti-cancer properties, (3beta,5xi)-lanosta-7,9(11)-dien-3-ol is used in the development of cancer treatments, targeting various types of cancer cells and contributing to the advancement of oncology research.
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.
2644-75-9Relevant 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).
