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(Z)-5-methyl-2-(3-nitrobenzylidene)benzofuran-3(2H)-one is a complex organic compound characterized by a benzofuran core, which is a fused ring system consisting of a benzene ring and a furan ring. The molecule features a methyl group at the 5-position, a nitro group on the 3-position of the benzylidene moiety, and a 2H-configuration indicating the presence of a hydrogen atom in a specific geometric arrangement. (Z)-5-methyl-2-(3-nitrobenzylidene)benzofuran-3(2H)-one is known for its potential applications in the field of chemistry, particularly in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

2567-72-8

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2567-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2567-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2567-72:
(6*2)+(5*5)+(4*6)+(3*7)+(2*7)+(1*2)=98
98 % 10 = 8
So 2567-72-8 is a valid CAS Registry Number.

2567-72-8Downstream Products

2567-72-8Relevant academic research and scientific papers

An unusual triazole synthesis from aurones

Kafle, Arjun,Bhattarai, Shrijiana,Handy, Scott T.

, p. 2337 - 2346 (2020)

Attempts to prepare azido-substituted aurones via a copper-catalyzed azidation failed to afford the desired product, but instead resulted in an unusual triazole formation reaction. Further efforts noted that copper was not required for this reaction, but simply thermal treatment with sodium azide in a polar aprotic solvent. A wide range of substitution patterns were tolerated in this reaction to afford the interesting salicyl-substituted triazoles in modest to excellent yield. While the mechanism is not yet clear, a simple elimination/cyclization pathway seems unlikely given the failure of the reaction on the corresponding thioaurones, which feature an even better thiol leaving group. Regardless, the potential utility of these easily accessible, multifunctional compounds should engender further interest and applications.

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