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Ethyl 2-(3-oxobutanamido)benzoate is a chemical compound with the molecular formula C13H15NO4. It is a derivative of benzoic acid, where the carboxylic acid group is esterified with ethanol, and the remaining part of the molecule contains an amide group attached to a 3-oxobutanoic acid chain. ethyl 2-(3-oxobutanamido)benzoate is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. It is characterized by its ability to form a stable amide linkage, which is crucial for its reactivity and utility in chemical transformations. The compound's structure and properties make it a valuable component in the development of new medications and therapeutic agents.

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Check Digit Verification of cas no

The CAS Registry Mumber 728-57-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 728-57:
(5*7)+(4*2)+(3*8)+(2*5)+(1*7)=84
84 % 10 = 4
So 728-57-4 is a valid CAS Registry Number.

728-57-4Relevant academic research and scientific papers

HFIP-mediated strategy towards β-oxo amides and subsequent Friedel-Craft type cyclization to 2?quinolinones using recyclable catalyst

Kabi, Arup K.,Gujjarappa, Raghuram,Vodnala, Nagaraju,Kaldhi, Dhananjaya,Tyagi, Ujjawal,Mukherjee, Kalisadhan,Malakar, Chandi C.

, (2020)

A simple and cost-effective 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP)-mediated protocol for the synthesis of β-oxo amides has been described by using amines and β-keto esters as substrates. The reaction conditions were found to be highly efficient towards the cleavage of C[sbnd]O bond and consequent formation of the products in excellent yields and selectivity. The obtained β-oxo amides were further transformed in to the synthetically useful 2?quinolinones via intramolecular Friedel-Craft type cyclization of aromatic ring using ferrites as a recyclable catalyst. A spectrum of substrates bearing broad range of functional groups were well tolerated under the reaction conditions. The proposed mechanistic pathways were substantially verified by literature and mass-spectroscopic evidences.

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