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(4-Methoxy-phenyl)-(2-phenyl-2H-quinolin-1-yl)-methanone is a complex organic compound with the molecular formula C25H19NO2. It is characterized by a methanone group (a carbonyl group attached to two carbon atoms), a 4-methoxy-phenyl group (a phenyl ring with a methoxy substituent at the 4-position), and a 2-phenyl-2H-quinolin-1-yl group (a quinoline ring with a phenyl substituent at the 2-position). (4-Methoxy-phenyl)-(2-phenyl-2H-quinolin-1-yl)-methanone is known for its potential applications in the field of pharmaceuticals and materials science, particularly in the development of new drugs and advanced materials. Its unique structure allows for a range of chemical properties and reactivity, making it a subject of interest for researchers in organic chemistry.

98847-85-9

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98847-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98847-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,4 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98847-85:
(7*9)+(6*8)+(5*8)+(4*4)+(3*7)+(2*8)+(1*5)=209
209 % 10 = 9
So 98847-85-9 is a valid CAS Registry Number.

98847-85-9Downstream Products

98847-85-9Relevant academic research and scientific papers

DUAL REACTIVITY OF 1,2-DISUBSTITUTED DIHYDRO-N-HETEROAROMATIC SYSTEMS. 6. ELECTROCHEMICAL OXIDATION OF N-ACYL DERIVATIVES OF 2-PHENYL-1,2-DIHYDROQUINOLINES

Sosonkin, I. M.,Sheinkman, A. K.,Vdovkina, G. G.,Chmilenko, T. S.,Domarev, A. N.

, p. 667 - 671 (2007/10/02)

In the electrochemical oxidation of 1-acyl-2-phenyl-1,2-dihydroquinolines, first the radical cations of the starting compounds form; these then lose a benzoyl radical and go over to the 2-arylquinoline cations.

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