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5397-53-5

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5397-53-5 Usage

General Description

Ethyl 2-acetyltetradecanoate is a chemical compound that belongs to the class of organic compounds known as fatty acid esters. It is a synthetic compound derived from ethyl alcohol and acetyltetradecanoic acid. This chemical is often used as a flavoring and fragrance ingredient due to its pleasant fruity and floral aroma. It is commonly used in the production of perfumes, soaps, and cosmetics. Additionally, ethyl 2-acetyltetradecanoate is also used in the food industry as a flavoring agent. However,

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.

5397-53-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-acetyltetradecanoate

1.2 Other means of identification

Product number -
Other names ethyl 2-n-dodecylacetoacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5397-53-5 SDS

5397-53-5Relevant articles and documents

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.

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