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1-Fluoro-4-((trifluoromethylsulfonyl)methyl)benzene is an organic compound characterized by a benzene ring with a fluorine atom at the 1st position and a trifluoromethylsulfonyl group attached to the 4th position through a methylene bridge. This molecule is a derivative of benzene, where the trifluoromethylsulfonyl group imparts unique reactivity and stability due to its electron-withdrawing and lipophilic properties. The compound is of interest in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals, as the trifluoromethylsulfonyl group can act as a protecting group or a leaving group in various chemical reactions. Its synthesis involves the introduction of the trifluoromethylsulfonyl group to a substituted benzene, which can be achieved through various methods, including electrophilic aromatic substitution. The compound's properties, such as its boiling point, solubility, and reactivity, are influenced by the presence of the electronegative fluorine and the bulky trifluoromethylsulfonyl groups, making it a versatile building block in the synthesis of more complex molecules.

2408-04-0

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2408-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2408-04-0 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 2408-04:
(6*2)+(5*4)+(4*0)+(3*8)+(2*0)+(1*4)=60
60 % 10 = 0
So 2408-04-0 is a valid CAS Registry Number.

2408-04-0Downstream Products

2408-04-0Relevant academic research and scientific papers

Copper-catalyzed direct trifluoromethylthiolation of benzylic C-H bonds via nondirected oxidative C(sp3)-H activation

Chen, Chao,Xu, Xiu-Hua,Yang, Bin,Qing, Feng-Ling

supporting information, p. 3372 - 3375 (2014/07/08)

A copper-catalyzed trifluoromethylthiolation of benzylic sp3 C-H bonds was developed via nondirected oxidative C-H activation using readily prepared and stable AgSCF3. This reaction provides a novel and straightforward method for the preparation of various benzyl trifluoromethyl sulfides.

Gas-phase acidities of α- and α,α-SO2CF 3-substituted toluenes. Varying Resonance demand in the electron-rich system

Zhang, Min,Badal, Md. Mizanur Rahman,Koppel, Ilmar A.,Mishima, Masaaki

, p. 813 - 820 (2013/08/15)

The gas-phase acidities (GA) of aryl(trifluoromethylsulfonyl)methanes (ArCH2SO2CF3; 1) and arylbis(trifluoromethylsulfonyl) methanes (ArCH(SO2CF 3)2; 2) were determined by measuring proton-

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