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1-(4-nitrophenacyl)-2-pyridone is a chemical compound with the molecular formula C12H8N2O4. It is a derivative of 2-pyridone, featuring a 4-nitrophenacyl group attached to the 1-position of the pyridone ring. 1-(4-nitrophenacyl)-2-pyridone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the preparation of certain antibiotics and other bioactive molecules. The 4-nitro group on the phenacyl moiety can be reduced to an amine group, which is a common step in the synthesis of certain drugs. The compound's structure and reactivity make it a valuable building block in organic chemistry, especially in the development of new therapeutic agents.

5517-84-0

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5517-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5517-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,1 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5517-84:
(6*5)+(5*5)+(4*1)+(3*7)+(2*8)+(1*4)=100
100 % 10 = 0
So 5517-84-0 is a valid CAS Registry Number.

5517-84-0Downstream Products

5517-84-0Relevant academic research and scientific papers

Heterocycles containing a bridge nitrogen atom. 10. Unexpected closure of oxazole ring during the reaction of 2-chloro-1-phenacylpyridinium salt with potassium cyanate. Crystal structure of 2-(p-nitrophenyl)oxazolo-[3,2-a]pyridinium bromide and N-(p-nitrophenacyl)pyrid-2-one

Babaev,Rybakov,Zhukov,Orlova

, p. 479 - 485 (1999)

Reaction of 2-chloro-N-(p-nitrophenacyl)pyridinium bromide with potassium cyanate in acetonitrile produces 2-(p-nitrophenyl)oxazolopyridinium bromide. Performing the same reaction in methanol N-(p-nitrophenacyl)pyrid-2-one was isolated. The structures of the obtained products were proved by X-ray structural data. 1999 KluwerAcademic/Plenum Publishers.

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