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1-phenoxy-2-<(trifluoromethyl)thio>benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131880-24-5

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131880-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131880-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,8 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131880-24:
(8*1)+(7*3)+(6*1)+(5*8)+(4*8)+(3*0)+(2*2)+(1*4)=115
115 % 10 = 5
So 131880-24-5 is a valid CAS Registry Number.

131880-24-5Relevant academic research and scientific papers

Power-variable electrophilic trifluoromethylating agents. S-, Se-, and Te-(trifluoromethyl)dibenzothio-, -seleno-, and -tellurophenium salt system

Umemoto, Teruo,Ishihara, Sumi

, p. 2156 - 2164 (1993)

S-, Se-, and Te-trifluoromethylated dibenzoheterocyclic onium salts, their derivatives, and related salts were synthesized by the direct fluorination of a mixture of 2-[(trifluoromethyl)thio- or seleno]biphenyls and triflic acid (TfOH) or HBF4 etherate, by treatment of the corresponding sulfoxides and selenoxides with Tf2O, by a new type of tellurium activation of 2-[(trifluoromethyl)telluro]biphenyl with Tf2O and (CH3)2SO, or by derivation from the onium salts obtained. Examination of reactivity indicated the trifluoromethyl heterocyclic salts to be greatly reactive compared to nonheterocyclic salts and indicated that this heterocyclic salt system serves as a source of widely applicable trifluoromethylating agents. Their capacity to function as such varied remarkably and increased in the order of Te 2 2. For mixed heterocyclic salts, the orders differed, apparently being determined by the electron deficiency of the CF3 group due to the electron-withdrawing or -donating effects of chalcogens and ring substituents, rather than the inherent nature of the chalcogens. Because of this variation, it was possible to trifluoromethylate a wide range of nucleophilic substrates differing in reactivity: carbanions, activated aromatics, heteroaromatics, enol silyl ethers, enamines, phosphines, thiolate anions, and iodide anions. The reaction mechanism is discussed, and a bimolecular ionic substitution mechanism competing with a free CF3 radical chain mechanism is proposed. Thus, a new field, electrophilic trifluoromethylation, has been established by the present study.

Perfluoroalkyl-containing compound

-

, (2008/06/13)

A (perfluoroalkyl)dibenzonium salt represented by the following general formula STR1 wherein Rf represents a perfluoroalkyl group having 1 to 10 carbon atoms, A represents a sulfur of selenium atom, R1 and R2, independentl

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