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1,4-bis(trifluoromethyl)-2,3,5-trifluorobenzene is a synthetic aromatic compound characterized by its unique molecular structure. It consists of a benzene ring with three fluorine atoms at the 2, 3, and 5 positions, and two trifluoromethyl groups attached at the 1 and 4 positions. 1,4-bis(trifluoromethyl)-2,3,5-trifluorobenzene is known for its high stability and resistance to chemical reactions due to the strong electron-withdrawing nature of the fluorine and trifluoromethyl groups. It is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and specialty materials, where its unique electronic properties and reactivity can be exploited. The compound's chemical formula is C8F10, and it is often referred to by its IUPAC name or a similar identifier in scientific literature and industrial settings.

2355-94-4

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2355-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2355-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2355-94:
(6*2)+(5*3)+(4*5)+(3*5)+(2*9)+(1*4)=84
84 % 10 = 4
So 2355-94-4 is a valid CAS Registry Number.

2355-94-4Downstream Products

2355-94-4Relevant academic research and scientific papers

Transformations of perfluoroxylenes and perfluoro-p-cymene under the action of Zn(Cu)-DMF-H2O

Krasnov, Vyacheslav I.,Platonov, Vyacheslav E.,Beregovaya, Irina V.,Shchegoleva, Lyudmila N.

, p. 1797 - 1812 (2007/10/03)

Perfluorinated xylenes and perfluoro-para-cymene undergo hydrodefluorination under the action of Zn(Cu)-DMF-H2O. Hydrogen enters mainly at the benzyl position of para-dialkylbenzenes and at the para position to perfluoroalkyl groups of perfluor

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