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2,2,3,3,4,4,5,5,6,6,6-Undecafluoro-1-phenylhexan-1-one is a complex organic compound characterized by its unique molecular structure. It is a derivative of hexanone, with the molecular formula C12H3F11O. 2,2,3,3,4,4,5,5,6,6,6-undecafluoro-1-phenylhexan-1-one is notable for its high fluorine content, with eleven fluorine atoms replacing hydrogen atoms in the molecule. The presence of these fluorine atoms significantly influences the compound's physical and chemical properties, such as its reactivity, stability, and lipophilicity. Due to its specific structure, it may have applications in various fields, including pharmaceuticals, materials science, and as a chemical intermediate. However, it is important to note that the compound's specific uses and properties would be determined by further research and development, as well as safety and environmental assessments.

308-06-5

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308-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 308-06-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 308-06:
(5*3)+(4*0)+(3*8)+(2*0)+(1*6)=45
45 % 10 = 5
So 308-06-5 is a valid CAS Registry Number.

308-06-5Downstream Products

308-06-5Relevant academic research and scientific papers

Photoredox-catalyzed redox-neutral difluoroalkylation to construct perfluoroketones with difluoroenoxysilanes

Lin, Wu-Jie,Liu, Xue-Yuan,Sun, Wen-Hui,Wang, Yu-Zhao,Zou, Jian-Yu

, p. 8696 - 8700 (2021/10/22)

A mild and facile approach to construct various perfluoroketonesviaphoto-catalyzed difluoroalkylation of difluoroenoxysilanes is developed. The reaction includes a strategy of combination of two fluorine-containing functional groups, which confers the reaction with characteristics like high efficiency, mild conditions, and broad scope. A variety of fluoroalkyl halides including perfluoroalkyl iodides, bromo difluoro esters and amides can be employed as radical precursors. Control experiments indicate that a single-electron transfer pathway may be involved in the reaction.

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