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1-Fluoro-3-(phenylsulfinyl)benzene is an organic compound characterized by the presence of a fluorine atom at the 1st position, a phenylsulfinyl group at the 3rd position, and a benzene ring. This molecule is a derivative of benzene, with a fluorine atom replacing one hydrogen atom and a phenylsulfinyl group replacing another. The phenylsulfinyl group consists of a sulfur atom bonded to a phenyl ring, which imparts unique chemical properties to the molecule. 1-fluoro-3-(phenylsulfinyl)benzene is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other specialty chemicals due to its unique structure and reactivity.

40154-92-5

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40154-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40154-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40154-92:
(7*4)+(6*0)+(5*1)+(4*5)+(3*4)+(2*9)+(1*2)=85
85 % 10 = 5
So 40154-92-5 is a valid CAS Registry Number.

40154-92-5Downstream Products

40154-92-5Relevant academic research and scientific papers

Direct C–H Carboxylation Forming Polyfunctionalized Aromatic Carboxylic Acids by Combined Br?nsted Bases

Hanasaka, Kazuya,Izumi, Koki,Kondo, Yoshinori,Kwon, Eunsang,Nozawa-Kumada, Kanako,Shigeno, Masanori,Tohara, Itsuki,Yamakoshi, Hiroyuki

supporting information, p. 809 - 814 (2022/02/05)

CO2 fixation into electron-deficient aromatic C–H bonds proceeds with the combined Br?nsted bases LiO-t-Bu and LiO-t-Am/CsF/18-crown-6 (t-Am = CEtMe2) under a CO2 atmosphere to afford a variety of polyfunctionalized aromat

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