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(3-fluorobenzyl)(trifluoromethyl)sulfane is a chemical compound with the molecular formula C8H7F3S. It is an organosulfur compound that features a sulfur atom bonded to a 3-fluorobenzyl group and a trifluoromethyl group. The 3-fluorobenzyl group consists of a benzene ring with a fluorine atom at the 3rd position and a methyl group attached to the benzene ring, while the trifluoromethyl group is a methyl group with three fluorine atoms. (3-fluorobenzyl)(trifluoromethyl)sulfane is known for its unique electronic properties due to the presence of fluorine atoms, which can influence its reactivity and stability. It may be used in the synthesis of various pharmaceuticals, agrochemicals, and materials science applications where its specific structural and electronic features are advantageous.

2408-08-4

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2408-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2408-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2408-08:
(6*2)+(5*4)+(4*0)+(3*8)+(2*0)+(1*8)=64
64 % 10 = 4
So 2408-08-4 is a valid CAS Registry Number.

2408-08-4Relevant academic research and scientific papers

An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes

Jiang, Min,Zhu, Fangxia,Xiang, Haoyue,Xu, Xing,Deng, Lianfu,Yang, Chunhao

, p. 6935 - 6939 (2015/06/25)

An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes was developed. The transformation employs only AgSCF3 and KI in situ generated active nucleophilic trifluoromethylthio species and cleanly occurs in up to quantitative yield at room temperature, thereby providing an unprecedentedly easy entry to various α-SCF3-substituted ketones/arylmethanes.

Room temperature nucleophilic trifluoromethylthiolation of benzyl bromides with (bpy)Cu(SCF3)

Kong, Dedao,Jiang, Zhou,Xin, Shaogang,Bai, Zhengshuai,Yuan, Yaofeng,Weng, Zhiqiang

, p. 6046 - 6050 (2013/07/27)

The nucleophilic trifluoromethylthiolation of benzyl bromides using (bpy)Cu(SCF3) gave the desired products of benzyl trifluoromethyl sulfides in good to excellent yields. A diverse set of important functional groups including cyano, nitro, ester, alkoxy, halide, and heterocyclic groups can be well tolerated in the protocol.

Trifluoro methylthiomethyl benzene derivatives and process for production same

-

, (2008/06/13)

The present invention lies in a process for producing a trifluoromethylthiomethylbenzene derivative represented by the following general formula (2): (wherein R is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group,

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