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2-Fluorotriphenylene is an organic compound with the molecular formula C18H11F. It is a derivative of triphenylene, a polycyclic aromatic hydrocarbon, where one hydrogen atom is replaced by a fluorine atom at the 2-position. This substitution imparts unique electronic and chemical properties to the molecule, making it a valuable building block in the synthesis of various fluorinated materials and compounds. 2-Fluorotriphenylene is used in the production of specialty polymers, pharmaceuticals, and other advanced materials due to its stability and reactivity. Its synthesis typically involves the fluorination of triphenylene or other related compounds, and it is often employed in research and development for its potential applications in areas such as electronics, materials science, and medicinal chemistry.

439-23-6

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439-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439-23-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 439-23:
(5*4)+(4*3)+(3*9)+(2*2)+(1*3)=66
66 % 10 = 6
So 439-23-6 is a valid CAS Registry Number.

439-23-6Downstream Products

439-23-6Relevant academic research and scientific papers

Atmosphere-Controlled Palladium-Catalyzed Divergent Decarboxylative Cyclization of 2-Iodobiphenyls and α-Oxocarboxylic Acids

Zhou, Liwei,Sun, Mingjie,Zhou, Fengru,Deng, Guobo,Yang, Yuan,Liang, Yun

, p. 7150 - 7155 (2021/09/18)

A novel palladium-catalyzed divergent decarboxylative cyclization of 2-iodobiphenyls and α-oxocarboxylic acids utilizing the atmosphere as a controlled switch is reported. Under the protection of a nitrogen atmosphere, tribenzotropones are synthesized by a [4 + 3] decarboxylative cyclization. Employing a palladium/O2 system enables a [4 + 2] decarboxylative cyclization to assemble triphenylenes. Notably, preliminary mechanistic studies indicate that the formation of triphenylenes involves a double decarboxylation.

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