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Benzene, 1,4-difluoro-2,3,5,6-tetrakis(phenylthio)-, also known as 1,4-difluorotetrakis(phenylthio)benzene, is a complex organic compound with the molecular formula C32H22F2S4. It is characterized by a benzene ring with two fluorine atoms at the 1 and 4 positions, and four phenylthio groups (phenylthio = C6H5-SH) attached to the 2, 3, 5, and 6 positions. Benzene, 1,4-difluoro-2,3,5,6-tetrakis(phenylthio)- is of interest in organic chemistry and materials science due to its unique structure and potential applications in the synthesis of various compounds and materials. It is typically synthesized through a series of chemical reactions and is used as a building block for more complex molecules or as a reagent in certain chemical processes.

2560-56-7

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2560-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2560-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2560-56:
(6*2)+(5*5)+(4*6)+(3*0)+(2*5)+(1*6)=77
77 % 10 = 7
So 2560-56-7 is a valid CAS Registry Number.

2560-56-7Relevant academic research and scientific papers

Crystal Multi-Conformational Control Through Deformable Carbon-Sulfur Bond for Singlet-Triplet Emissive Tuning

Wu, Hongwei,Chi, Weijie,Baryshnikov, Gleb,Wu, Bin,Gong, Yifan,Zheng, Dongxiao,Li, Xin,Zhao, Yanli,Liu, Xiaogang,?gren, Hans,Zhu, Liangliang

supporting information, p. 4328 - 4333 (2019/03/11)

Crystal-state luminophores have been of great interest in optoelectronics for years, whereas the excited state regulation at the crystal level is still restricted by the lack of control ways. We report that the singlet-triplet emissive property can be pro

Potassium Cryptate of a Macrobicyclic Ligand Featuring a Reducible Hexakis(phenylthio)benzene Electron-Acceptor Site

Mayor, Marcel,Lehn, Jean-Marie

, p. 2277 - 2285 (2007/10/03)

The synthesis and structural characterization of the macrobicyclic ligand 1 containing a reducible hexakis(phenylthio)benzene electron-acceptor site is described. It is based on the condensation of the tetraoxa-di-azamacrocycle 3 with a suitably functiona

THE THIOLATE ANION AS A NUCLEOPHILE. PART XIV. FURTHER REACTIONS OF TIN(II) ARENETHIOLATES

Jesudason, J. Joseph,Peach, Michael E.

, p. 357 - 362 (2007/10/02)

The reactions of tin(II) benzenethiolate in DMF with hexafluorobenzene, chloropentafluorobenzene and bromopentafluorobenzene have been compared.Replacement of fluorine and chlorine by the phenylthio group and protodebromination were observed.DMF was a better solvent than either ethylene glycol/pyridine mixture (1:2) or diglyme for the reaction.New products have been isolated and characterized from the reactions of tin(II) p-chlorobenzenethiolate with hexafluorobenzene, decafluorobiphenyl, octafluorotoluene and pentafluorobenzyl bromide.

THE THIOLATE ANION AS A NUCLEOPHILE. PART XIII. REACTIONS OF SOME TIN(II) AROMATIC THIOLATES

Hynes, Rosemary C.,Peach, Michael E.

, p. 129 - 134 (2007/10/02)

The reactions of tin(II) benzenethiolate and p-toluenethiolate with various fluoroaromatics in DMF have been studied.Replacement of some of the aromatic fluorines by the thiolate group was observed.The tin(II) aromatic thiolates are comparable in reactivity in these reactions with lead(II) benzenethiolate.All new compound have been characterized by elemental analysis, and NMR (H-1 and F-19) and mass spectroscopy.

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