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4-((4-fluorophenyl)sulfonyl)-1,1′-biphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30745-09-6

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30745-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30745-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,4 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30745-09:
(7*3)+(6*0)+(5*7)+(4*4)+(3*5)+(2*0)+(1*9)=96
96 % 10 = 6
So 30745-09-6 is a valid CAS Registry Number.

30745-09-6Downstream Products

30745-09-6Relevant academic research and scientific papers

Synthesis of Sulfones via Ru(II)-Catalyzed Sulfination of Boronic Acids

Gulbe, Krista,Turks, Mā ris

, p. 5660 - 5669 (2020/05/19)

Ruthenium(II) complexes catalyze the insertion of sulfur dioxide into (het)aryl and alkenyl boronic acids. The transmetalation-sulfination process proceeds with DABSO in the presence of 5 mol % RuCl2(PPh3)3 in methanol at 100 °C. The intermediate sulfinate salt can be quenched with various electrophiles such as alkyl halides, epoxides, Michael acceptors, and λ3-iodanes in moderate to good yields. The reported sulfone synthesis can be performed either as a direct one-pot or one-pot two-step procedure depending on the reactivity of the electrophile.

Preparation process of fluorine substituted aromatic compound

-

, (2008/06/13)

A preparation process of a fluorine substituted aromatic compound comprising reacting an alkali metal or alkali earth metal salt of an aromatic compound having a hydroxy group with an organic fluorinating agent is disclosed. As a representative fluorinating agent, a bis-dialkylamino-difluoromethane compound, for example, 2,2′-difluoro-1,3-dimethylimidazolidine, is exemplified. According to the process, an industrially useful fluorinated aromatic compound, for example, a fluorobenzene, a fluorine substituted benzophenone, a fluorine substituted diarylsulfone can be prepared with ease in economy without specific equipment.

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