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(4-Methoxyphenyl)(3-methylquinoxalin-2-yl)methanone is a complex organic compound with the molecular formula C17H14N2O2. It is characterized by a quinoxaline-2-yl group, which is a fused bicyclic structure consisting of a benzene ring and a diazine ring, and a 4-methoxyphenyl group, which is a phenyl ring with a methoxy substituent at the para position. The compound features a central methanone group, which is a carbonyl group (C=O) bonded to a methyl group. This molecule is known for its potential applications in pharmaceutical research, particularly in the development of compounds with biological activity. Its structure provides a basis for further chemical modifications and exploration of its properties in various scientific and medical contexts.

23773-97-9

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23773-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23773-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,7 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23773-97:
(7*2)+(6*3)+(5*7)+(4*7)+(3*3)+(2*9)+(1*7)=129
129 % 10 = 9
So 23773-97-9 is a valid CAS Registry Number.

23773-97-9Downstream Products

23773-97-9Relevant academic research and scientific papers

REACTION OF BENZOFURAZAN 1-OXIDE WITH 1-(2-NAPHTHYL)- AND 1-HETARYL-BUTANE-1,3-DIONES; PREPARATION OF ARYL AND HETARYL 2-QUINOXALINYL KETONES

Athaf, Adnan,Hill, John

, p. 4557 - 4564 (1989)

Aryl (4-methoxyphenyl and 2-naphthyl) and hetaryl (2-furyl, 3-pyridyl and 2-thienyl) 3-methyl-2-quinoxalinyl ketones were prepared via the reaction of benzofurazan 1-oxide (BFO) with 1-aryl and 1-hetaryl-butane-1,3-diones, followed by reduction of the res

Metal-, Photocatalyst-, and Light-Free Direct C-H Acylation and Carbamoylation of Heterocycles

Westwood, Matthew T.,Lamb, Claire J. C.,Sutherland, Daniel R.,Lee, Ai-Lan

, p. 7119 - 7123 (2019/09/03)

Direct C-H acylations and carbamoylations of heterocycles can now be readily achieved without requiring any conventional metal, photocatalyst, electrocatalysis, or light activation, thus significantly improving on sustainability, costs, toxicity, waste, and simplicity of the operational procedure. These mild conditions are also suitable for gram-scale reactions and late-stage functionalizations of complex molecules, including pharmaceuticals, N,N-ligands, and light-sensitive molecules.

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