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2,3,5,6-Tetrafluoro-N1,N1,N4,N4-tetramethyl-1,4-benzenediamine is a complex organic compound characterized by its unique molecular structure. It features a benzene ring with two amine groups (-NH2) attached to the 1 and 4 positions, and four fluorine atoms substituting the hydrogen atoms at the 2, 3, 5, and 6 positions. The compound also has two methyl groups (-CH3) attached to each of the amine nitrogen atoms, which contribute to its stability and reactivity. This chemical is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its specific electronic and steric properties. Its synthesis and use often involve advanced organic chemistry techniques, and it may be a component in the development of new compounds with specialized functions.

2262-15-9

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2262-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2262-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2262-15:
(6*2)+(5*2)+(4*6)+(3*2)+(2*1)+(1*5)=59
59 % 10 = 9
So 2262-15-9 is a valid CAS Registry Number.

2262-15-9Relevant academic research and scientific papers

MULTI-ELECTRON REDOX ACTIVE MOLECULES FOR ENERGY STORAGE APPLICATIONS

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Paragraph 0114; 0115, (2017/03/21)

A non-aqueous redox flow battery includes a catholyte including a compound of formula (I) or a compound of formula (II): Where X1 is a moiety of formula I-A or I-B:

Reactions of HMPA with hexafluorobenzene, pentafluorochlorobenzene and pentafluorophenol

Zhang, Cheng-Pan,Chen, Qing-Yun,Xiao, Ji-Chang

, p. 424 - 428 (2008/12/22)

Hexamethylphophoramide (HMPA) reacted with hexafluorobenzene and its derivatives with good conversion to give dimethylaminated products and phosphorofluoridates, even in unfavorable reaction stoichiometries. An aromatic nucleophilic mechanism might be inv

Preparation of dialkylamino-substituted benzenes and naphthalenes by nucleophilic replacement of fluorine in the corresponding perfluoroaromatic compounds

Sorokin, Vladimir I.,Ozeryanskii, Valery A.,Borodkin, Gennady S.,Chernyshev, Anatoly V.,Muir, Max,Baker, Jon

, p. 615 - 625 (2008/01/27)

The reactions between hexafluorobenzene (HFB) and octafluoronaphthalene (OFN) with secondary aliphatic amines (pyrrolidine, dimethylamine and piperidine) and lithium amides (pyrrolidide, dimethylamide and piperidide) have been investigated both experiment

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