13985-56-3 Usage
General Description
2-Ethyl-1,3-dinitrobenzene is an organic compound with the chemical formula C8H8N2O4. It is a yellow solid that is used as an intermediate in the production of dyes and other organic compounds. 2-Ethyl-1,3-dinitrobenzene is considered to be toxic and a potential irritant to the skin, eyes, and respiratory system. Its primary use is in the synthesis of various aromatic compounds and dyes, and it is also utilized as a pesticide. It is important to handle this chemical with caution and follow proper safety protocols when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 13985-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,8 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13985-56:
(7*1)+(6*3)+(5*9)+(4*8)+(3*5)+(2*5)+(1*6)=133
133 % 10 = 3
So 13985-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O4/c1-2-6-7(9(11)12)4-3-5-8(6)10(13)14/h3-5H,2H2,1H3
13985-56-3Relevant articles and documents
NITRATION OF AROMATIC COMPOUNDS
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Paragraph 0049, (2016/08/17)
The present invention provides a process for nitrating aromatic compounds without the need for a solid catalyst and/or any organic solvents and/or any other additives. A typical process includes combining or admixing a nitric acid and an anhydride compound under conditions sufficient to produce a reactive intermediate. The aromatic compound to be nitrated is then added to this reactive intermediate to produce a nitroaromatic compound. The nitroaromatic compound can be substituted with one or more, typically, one to three, and often one or two nitrate (-NO2) groups.
Preparation of 8-alkyl 7-(2-imidazolinylamino)quinolines via palladium mediated alkylations
Nikolaides, Nick,Bogdan, Sophie E.,Szalma, James S.
, p. 2027 - 2033 (2007/10/03)
A convenient preparation of 8-alkyl substituted 7-(2-imidazo linylamino)quinolines from the corresponding 8-trifluoro-methanesulfonates, utilizing palladium cross-coupling reactions is described.
