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1-Phenylthio-4-trifluoromethyl-tetrafluoro-benzene is a complex organic compound characterized by its unique molecular structure. It features a benzene ring with four fluorine atoms, one phenylthio group, and one trifluoromethyl group. The phenylthio group is attached to the first carbon of the benzene ring, while the trifluoromethyl group is attached to the fourth carbon. 1-phenylthio-4-trifluoromethyl-tetrafluoro-benzene is known for its stability and unique chemical properties, which make it a potential candidate for various applications in the fields of pharmaceuticals, materials science, and chemical research. Its specific structure and properties can be further explored for potential uses in the development of new drugs, advanced materials, or as an intermediate in the synthesis of other complex molecules.

1548-86-3

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1548-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1548-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1548-86:
(6*1)+(5*5)+(4*4)+(3*8)+(2*8)+(1*6)=93
93 % 10 = 3
So 1548-86-3 is a valid CAS Registry Number.

1548-86-3Relevant academic research and scientific papers

LADDER POLYMERS WITH INTRINSIC MICROPOROSITY AND PROCESS FOR PRODUCTION THEREOF

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Page/Page column 14-15; 20, (2010/05/14)

A polymer of formula (I): where: n is an integer from 10 to 5,000; m is an integer from 10 to 5,000; Ar1 and Ar3 are the same or different and are residues derived from a tetra-hydroxy aromatic monomer, the tetra-hydroxy aromatic monomer being wherein R i

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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