5397-53-5 Usage
Uses
Used in Perfumery and Fragrance Industry:
Ethyl 2-acetyltetradecanoate is utilized as a flavoring and fragrance ingredient due to its pleasant and appealing scent. It is incorporated into the production of perfumes to enhance their aromatic profiles, providing a fruity and floral note that contributes to the overall scent experience.
Used in Cosmetics Industry:
In the cosmetics industry, ethyl 2-acetyltetradecanoate serves as a key ingredient for adding fragrance to various products such as soaps, lotions, and creams. Its ability to impart a pleasant aroma makes it a valuable addition to these products, enhancing their sensory appeal and consumer acceptance.
Used in Food Industry:
Ethyl 2-acetyltetradecanoate is also employed as a flavoring agent in the food industry. Its fruity and floral notes can be used to add depth and complexity to a variety of food products, enhancing their taste and aroma profiles. This makes it a versatile ingredient for food manufacturers looking to create unique and appealing flavors in their offerings.
While the provided materials do not specify other industries or applications, the above uses are inferred based on the information given about ethyl 2-acetyltetradecanoate's properties and common uses in similar compounds within the fragrance and flavoring sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 5397-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5397-53:
(6*5)+(5*3)+(4*9)+(3*7)+(2*5)+(1*3)=115
115 % 10 = 5
So 5397-53-5 is a valid CAS Registry Number.
5397-53-5Relevant academic research and scientific papers
Synthesis of novel 1-hydroxyquinolones with high anti-toxoplasma activity
Tietze, Lutz F.,Ma, Ling
supporting information; experimental part, p. 377 - 396 (2011/04/24)
All for the treatment of malaria and toxoplasmosis the novel hydroxyquinolones 2-5 were prepared by reaction of aniline and hydroxyaniline, respectively and the β-ketoesters 10a-c. As products the quinolones 8 and 15, respectively were obtained. Benzylation, oxidation and hydrogenation then led to the desired substances. Compound 2 has a similar anti-malaria activity as the approved drug Atovaquone. The Japan Institute of Heterocyclic Chemistry.
