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"Benzene, [[(trifluoromethyl)sulfinyl]methyl]-" is a chemical compound with the molecular formula C8H7F3OS. It is an organic molecule that features a benzene ring with a unique functional group attached to it. The functional group in question is a (trifluoromethyl)sulfinyl group, which is connected to a methylene (-CH2-) bridge that is in turn attached to the benzene ring. Benzene, [[(trifluoromethyl)sulfinyl]methyl]- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique reactivity and stability. It is also recognized for its role as an intermediate in the production of certain specialty chemicals. The trifluoromethyl group provides electron-withdrawing properties, which can influence the reactivity and physical properties of the molecule, making it a valuable building block in organic synthesis.

4854-99-3

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4854-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4854-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4854-99:
(6*4)+(5*8)+(4*5)+(3*4)+(2*9)+(1*9)=123
123 % 10 = 3
So 4854-99-3 is a valid CAS Registry Number.

4854-99-3Downstream Products

4854-99-3Relevant academic research and scientific papers

Trifluoromethyl Sulfoxides: Reagents for Metal-Free C?H Trifluoromethylthiolation

Carlton, C. Grace,McDouall, Joseph J. W.,Perry, Gregory J. P.,Procter, David J.,Tayu, Masanori,Wang, Dong

, p. 15918 - 15922 (2020/07/20)

Trifluoromethyl sulfoxides are a new class of trifluoromethylthiolating reagent. The sulfoxides engage in metal-free C?H trifluoromethylthiolation with a range of (hetero)arenes. The method is also applicable to the functionalization of important compound classes, such as ligand derivatives and polyaromatics, and in the late-stage trifluoromethylthiolation of medicines and agrochemicals. The isolation and characterization of a sulfonium salt intermediate supports an interrupted Pummerer reaction mechanism.

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