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2-aminotetrafluorophenyl-pentafluorophenylsulfane is a complex organic chemical compound with the molecular formula C12H3F9NS. It is characterized by the presence of two aromatic rings, one being a 2-aminotetrafluorophenyl group and the other a pentafluorophenyl group, connected by a sulfane (sulfur-hydrogen) bridge. 2-aminotetrafluorophenyl-pentafluorophenylsulfane is known for its unique electronic properties due to the presence of fluorine atoms, which can influence its reactivity and stability. It is typically used in the synthesis of various fluorinated compounds and may have applications in the fields of pharmaceuticals, materials science, and chemical research. The compound's structure and properties make it a valuable intermediate in the development of new molecules with specific functionalities.

4997-44-8

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4997-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4997-44-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4997-44:
(6*4)+(5*9)+(4*9)+(3*7)+(2*4)+(1*4)=138
138 % 10 = 8
So 4997-44-8 is a valid CAS Registry Number.

4997-44-8Relevant academic research and scientific papers

Overcharge protection of lithium-ion batteries above 4 v with a perfluorinated phenothiazine derivative

Kaur, Aman Preet,Casselman, Matthew D.,Elliott, Corrine F.,Parkin, Sean R.,Risko, Chad,Odom, Susan A.

, p. 5410 - 5414 (2016/05/24)

Electron-withdrawing substituents are introduced onto the phenothiazine core to raise its oxidation potential for use as a redox shuttle in high-voltage lithium-ion batteries. A perfluorinated derivative oxidizes at 4.3 V vs. Li+/0, and functio

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