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2-(2,4-dinitrophenyl)-4-isopropyl-2-phenyl-5(2H)-oxazolone is a complex organic compound with the molecular formula C18H15N3O6. It is characterized by a 5(2H)-oxazolone ring, which is a five-membered heterocyclic ring containing two oxygen atoms and one nitrogen atom. The compound features a 2,4-dinitrophenyl group attached to the oxazolone ring, which contributes to its chemical reactivity and properties. Additionally, it has an isopropyl group and a phenyl group, which further influence its structure and potential applications. 2-(2,4-dinitrophenyl)-4-isopropyl-2-phenyl-5(2H)-oxazolone may be of interest in chemical research and development, particularly in areas such as pharmaceuticals or materials science, due to its unique structure and potential reactivity.

50709-69-8

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50709-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50709-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,0 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50709-69:
(7*5)+(6*0)+(5*7)+(4*0)+(3*9)+(2*6)+(1*9)=118
118 % 10 = 8
So 50709-69-8 is a valid CAS Registry Number.

50709-69-8Relevant academic research and scientific papers

5-Oxazolones, II 2,4-Diaryl-4-(2,4-dinitroaryl)-5(4H)-oxazolones: Synthesis and Acid-Catalyzed Transformation into 1-Hydroxy-1H-indazole Derivatives

D'Anello, Matteo,Erba, Emanuela,Gelmi, Maria Luisa,Pocar, Donato

, p. 67 - 74 (2007/10/02)

2,4-Diaryl-4-(2,4-dinitroaryl)-5(4 H)-oxazolones 2 were prepared by arylation of the corresponding 5(4H)-oxazolones 1 under phase-transfer conditions with the corresponding 1-halo-2,4-dinitrobenzenes. 2,4-Diaryl-4-(3,5-dinitro-2-pyridyl)-5(4H)-oxazolones 5 were obtained similarly from the corresponding 1 and 2-chloro-3,5-dinitropyridine.On reaction with methanol and p-toluenesulfonic acid , oxazolones 2 rearranged to the corresponding 1-hydroxy-1H-indazole derivatives 8.Under the same conditions oxazolones 5 afforded a mixture of the correspondingly substituted 1H-pyrazolopyridines 7 and substituted imidazopyridines 12.In all cases the solvolysis reaction, yielding substituted glycine esters 9 and 11, was competitive with the rearrangement.Reaction path are discussed.

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