27174-71-6 Usage
Description
Methyl 2-(1-adamantyl)acetate is a chemical compound that belongs to the class of organic compounds known as esters. It is derived from the reaction between 2-(1-adamantyl)acetic acid and methanol. This ester is characterized by its pleasant odor and taste, which makes it a valuable component in various applications.
Uses
Used in Fragrance and Flavor Industry:
Methyl 2-(1-adamantyl)acetate is used as a flavoring agent for its pleasant taste, enhancing the sensory experience of food products. Its aromatic properties also make it a popular ingredient in perfumes and other scented products, where it contributes to creating appealing and complex fragrances.
Used in Pharmaceutical Applications:
Methyl 2-(1-adamantyl)acetate is studied for its potential anti-inflammatory and anti-cancer properties. This research indicates that it may have therapeutic applications, particularly in the development of treatments for inflammatory conditions and various types of cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 27174-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,7 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27174-71:
(7*2)+(6*7)+(5*1)+(4*7)+(3*4)+(2*7)+(1*1)=116
116 % 10 = 6
So 27174-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-15-12(14)8-13-5-9-2-10(6-13)4-11(3-9)7-13/h9-11H,2-8H2,1H3
27174-71-6Relevant articles and documents
Aerosol Fluorination of 1-Chloroadamantane, 2-Chloroadamantane, and Methyl 1-Adamantylacetate: A Novel Synthetic Approach to 1- and 2-Substituted Hydryl-, Methyl, and (Difluoromethyl)-F-adamantanes
Adcock, James L.,Luo, Huimin,Zuberi, Sharique S.
, p. 4749 - 4752 (1992)
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Preparative synthesis of vinyl diamondoids
Fokin, Andrey A.,Butova, Ekaterina D.,Barabash, Anastasiya V.,Huu, Nhan N.,Tkachenko, Boryslav A.,Fokina, Natalie A.,Schreiner, Peter R.
, p. 1772 - 1777 (2013/05/21)
We describe a convenient four-step preparation of 1-vinyl adamantane, 1-vinyl diamantane, and 4,9-divinyl diamantane from the respective diamondoid acetic acids in 50-80% isolated yields involving esterification, reduction, and hydrobromination/dehydrobromination. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.
AZEPINE DERIVATIVES AND USE THEREOF
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, (2008/06/13)
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