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N-Acetyl-2-benzoyl-2-phenylacetamid is a complex organic compound with the chemical formula C17H15NO3. It is a derivative of acetamide, featuring a benzoyl group attached to a phenyl ring, which is further connected to another phenyl ring through an amide linkage. This molecule is known for its potential applications in pharmaceutical research, particularly in the development of new drugs, due to its unique structure and reactivity. It is synthesized through a series of chemical reactions, often involving the acylation of an appropriate precursor molecule. The compound's properties, such as its solubility and stability, can be influenced by the specific arrangement of its functional groups and the electronic effects they exert on each other. N-Acetyl-2-benzoyl-2-phenylacetamid is typically analyzed and studied in a laboratory setting to understand its chemical behavior and potential therapeutic applications.

7733-49-5

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7733-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7733-49-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7733-49:
(6*7)+(5*7)+(4*3)+(3*3)+(2*4)+(1*9)=115
115 % 10 = 5
So 7733-49-5 is a valid CAS Registry Number.

7733-49-5Relevant academic research and scientific papers

New Syntheses of 1,3-Oxazines, Thiazoles, and 1,2-Dithioles

Capuano, Lilly,Bolz, Gerda,Burger, Robert,Burkhardt, Volker,Huch, Volker

, p. 239 - 243 (2007/10/02)

The 2-diazo-1,3-diketones 1 react with thioamides 4 via the acyl ketenes 3, resulting from Wolff rearrangement, to give the 1,3-oxazine-4-ones 10; however, by increasing the electrophilicity of the diazo compounds or the nucleophilicity of the thioamides,

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