75672-24-1 Usage
Description
7-O-Acetyl Ursodeoxycholic Acid Methyl Ester is a chemical compound derived from ursodeoxycholic acid, a naturally occurring bile acid found in the bile of bears. It is characterized by its off-white foam appearance and is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
7-O-Acetyl Ursodeoxycholic Acid Methyl Ester is used as a reactant for the preparation of bile acids, specifically 3β-Ursodeoxycholic Acid. This application is crucial in the development of medications that target and treat various liver-related conditions, such as cholestasis and gallstones, by improving bile flow and reducing the formation of cholesterol stones.
Used in Chemical Synthesis:
7-O-Acetyl Ursodeoxycholic Acid Methyl Ester serves as an essential intermediate in the synthesis of other related compounds with potential applications in the pharmaceutical, cosmetic, and other industries. Its unique chemical structure allows for further modification and functionalization, leading to the creation of novel molecules with specific properties and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 75672-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,7 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75672-24:
(7*7)+(6*5)+(5*6)+(4*7)+(3*2)+(2*2)+(1*4)=151
151 % 10 = 1
So 75672-24-1 is a valid CAS Registry Number.
75672-24-1Relevant articles and documents
Preparation method of 3beta-ursodesoxycholic acid
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, (2019/07/04)
The invention discloses a synthesis method of 3beta-ursodesoxycholic acid. The method comprises following steps: ursodesoxycholic acid is taken as a raw material and subjected to esterification, 3-position and 7-position hydroxyl groups, selective removal of a 3-position protecting group, oxidization of the 3-position hydroxyl group, reduction into 3beta hydroxyl group and hydrolysis of 7-positionand 24-position hydroxyl groups, and 3beta-ursodesoxycholic acid is obtained. The synthesis method is novel, lower in cost, high in yield, simple and convenient to operate and environmentally friendly, and conditions are mild.
