42273-76-7 Usage
Description
VINYLBENZYL ALCOHOL, also known as α-Vinylbenzyl alcohol, is an allyl alcohol derivative with versatile chemical properties. It has been the subject of various research studies, including isomerization, asymmetric epoxidation, and coupling reactions. These reactions have been explored using different catalyst systems, such as tungsten, ruthenium, and ionic liquids, as well as immobilized sulfonic catalysts on silica.
Uses
Used in Chemical Synthesis:
VINYLBENZYL ALCOHOL is used as a key intermediate in the synthesis of various organic compounds, particularly cinnamyl ethers, by reacting with alcohols. This application is significant in the production of chemicals with diverse applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, VINYLBENZYL ALCOHOL is used as a building block for the development of new drugs and pharmaceutical compounds. Its unique chemical properties make it a valuable component in the synthesis of various therapeutic agents.
Used in Catalyst Research:
VINYLBENZYL ALCOHOL is used as a test substrate in the study of novel catalyst systems, such as tungsten-catalyzed asymmetric epoxidation and ruthenium-catalyzed coupling reactions. These studies contribute to the advancement of catalytic technologies and the development of more efficient and selective chemical processes.
Used in Material Science:
In the field of material science, VINYLBENZYL ALCOHOL is used in the development of new materials with specific properties. Its ability to undergo various chemical reactions allows for the creation of materials with tailored characteristics for specific applications.
Used in Green Chemistry:
VINYLBENZYL ALCOHOL is used in the development of environmentally friendly chemical processes, such as the etherification reaction with glycerol in the presence of an immobilized sulfonic catalyst on silica. This application contributes to the reduction of waste and the use of more sustainable chemical processes.
Synthesis Reference(s)
The Journal of Organic Chemistry, 52, p. 3524, 1987 DOI: 10.1021/jo00392a006
Check Digit Verification of cas no
The CAS Registry Mumber 42273-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,7 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42273-76:
(7*4)+(6*2)+(5*2)+(4*7)+(3*3)+(2*7)+(1*6)=107
107 % 10 = 7
So 42273-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O/c1-2-8-5-3-4-6-9(8)7-10/h2-6,10H,1,7H2
42273-76-7Relevant articles and documents
EFFICIENT RESOLUTION OF SECONDARY ALCOHOLS, CYANOHYDRINS, AND GLYCEROL ACETALS BY COMPLEXATION WITH THE HOST DERIVED FROM TARTARIC ACID
Toda, Fumio,Matsuda, Shotaro,Tanaka, Koichi
, p. 983 - 986 (2007/10/02)
Some title hydroxy compounds were resolved efficiently by complexation with the host compounds derived from tartaric acid.
