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4,5,6,7-tetrafluoro-2-phenylbenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34073-34-2

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34073-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34073-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,7 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34073-34:
(7*3)+(6*4)+(5*0)+(4*7)+(3*3)+(2*3)+(1*4)=92
92 % 10 = 2
So 34073-34-2 is a valid CAS Registry Number.

34073-34-2Relevant academic research and scientific papers

Palladium-catalyzed decarboxylative a polyfluoroarylation of ketones

Doi, Ryohei,Hayashi, Kanako,Sato, Yoshihiro

, p. 1181 - 1183 (2021/06/06)

Herein, we report palladium-catalyzed decarboxylative a-polyfluoroarylation of ketones. As a result of reaction condition screening, XPhos and Ruphos were selected as ancillary ligands for Pd(0) catalysts. The reaction was applied to a variety of substrates. A cross-over experiment was conducted to gain insight into the reaction mechanism.

Synthesis of polyfluorinated benzofurans

Politanskaya, Larisa,Troshkova, Nadezhda,Tretyakov, Evgeny,Xi, Chanjuan

, (2019/09/18)

A simple and efficient approach to the synthesis of fluorinated benzofurans including the Sonogashira cross-coupling of o-iodophenols with terminal Ph- and n-Bu-acetylenes, followed by intramolecular cyclization, in good to excellent yields is reported.

Photocatalytic hydrodefluorination: Facile access to partially fluorinated aromatics

Senaweera, Sameera M.,Singh, Anuradha,Weaver, Jimmie D.

supporting information, p. 3002 - 3005 (2014/03/21)

Polyfluorinated aromatics are essential to materials science as well as the pharmaceutical and agrochemical industries and yet are often difficult to access. This Communication describes a photocatalytic hydrodefluorination approach which begins with easily accessible perfluoroarenes and selectively reduces the C-F bonds. The method allows facile access to a number of partially fluorinated arenes and takes place with unprecedented catalytic activity using a safe and inexpensive amine as the reductant.

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