5409-32-5 Usage
Uses
Used in Dye and Pigment Production:
2-Ethylnaphthalene-1,4-dione is utilized as a key intermediate in the production of dyes and pigments. Its chemical properties allow it to contribute to the color and stability of these products, making it an essential component in this industry.
Used in Chemical Reactions and Processes:
Due to its reactivity, 2-ethylnaphthalene-1,4-dione is employed in a variety of chemical reactions and processes. Its ability to participate in different chemical transformations makes it a useful compound for creating new substances and improving existing ones.
Used in Pharmaceutical Development:
2-Ethylnaphthalene-1,4-dione may have potential uses in the pharmaceutical industry. Its unique chemical properties could be harnessed for the development of new drugs or the enhancement of existing ones, contributing to advancements in medicine.
Used in Organic Chemistry Research:
As a versatile compound in organic chemistry, 2-ethylnaphthalene-1,4-dione is also used in research settings. Scientists and researchers explore its properties and reactions to gain a deeper understanding of organic chemistry and to discover new applications for 2-ethylnaphthalene-1,4-dione.
Check Digit Verification of cas no
The CAS Registry Mumber 5409-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5409-32:
(6*5)+(5*4)+(4*0)+(3*9)+(2*3)+(1*2)=85
85 % 10 = 5
So 5409-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O2/c1-2-8-7-11(13)9-5-3-4-6-10(9)12(8)14/h3-7H,2H2,1H3
5409-32-5Relevant academic research and scientific papers
Reductive-alkylation and aromatic coupling reactions of 1,4-benzoquinone derivatives promoted by ethylaluminum dichloride
Ferreira, Vitor F.,Schmitz, Francis J.
, p. 1 - 6 (2007/10/03)
Reactions of several substituted 1,4-benzoquinones with ethylaluminum dichloride in dichloromethane were studied. It was found that some quinones undergo a new radical aromatic coupling under these conditions, while others undergo a 1,6-reductive O-alkylation.
ELECTRON-TRANSFER PROCESSES: MECHANISMS OF OXIDATION OF ETHERS AND ESTERS BY SILVER-CATALYZED PEROXYDISULPHATE
Minisci, Francesco,Coppa, Fausta,Fontana, Francesca,Zhao, Lihua
, p. 613 - 616 (2007/10/02)
Nucleophilic carbon-centred radicals, generated from the oxidation of diethyl ether, ethyl acetate, propyl acetate, ethyl propionate, diethyl oxalate and 2-phenylethyl acetate by silver-catalyzed decomposition of peroxydisulphate, have been trapped, mostly by naphthoquinone and in a few cases by protonated quinoline. Characterization of the intermediate radicals allows the rationalization of the mechanism of these oxidations, which are likely to occur through an initial electron-transfer step by Ag(II).
