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Ethyl 2-(4-methoxyphenylazo)-2-methyl-3-oxobutanoate is a complex organic compound with the chemical formula C14H17NO4. It is a derivative of azo compounds, characterized by the presence of an azo group (-N=N-) bonded to a 4-methoxyphenyl group. ethyl 2-(4-methoxyphenylazo)-2-methyl-3-oxobutanoate features a 2-methyl-3-oxobutanoate moiety, which is a four-carbon chain with a ketone group at the third carbon and a methyl group at the second carbon. The ethyl group is attached to the 2-carbon of the 3-oxobutanoate chain. Ethyl 2-(4-methoxyphenylazo)-2-methyl-3-oxobutanoate is known for its potential applications in the synthesis of dyes and pigments, as well as in various chemical research and industrial processes. Its molecular structure and properties make it a versatile building block in the field of organic chemistry.

4792-56-7

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4792-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4792-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4792-56:
(6*4)+(5*7)+(4*9)+(3*2)+(2*5)+(1*6)=117
117 % 10 = 7
So 4792-56-7 is a valid CAS Registry Number.

4792-56-7Relevant academic research and scientific papers

Process development of 5-methoxy-1H-indole-2-carboxylic acid from ethyl 2-methylmalonate

Bessard, Yves

, p. 214 - 220 (2013/09/08)

Development is described of a new process for the preparation from malonates of 5-methoxy-1H-indole-2-carboxylic acid esters, useful intermediates in the synthesis of pharmaceutical compounds. The process uses readily available starting materials, produces little waste, can be operated safely on at least 1 molar scale, and gives high yields. The main areas of optimization included the azo coupling of a diazonium salt with malonate derivatives, the Japp-Klingemann rearrangement, and the Fischer indole synthesis.

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