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2-phenyl-N-(phenylcarbamoyl)acetamide is an organic compound with the molecular formula C15H14N2O2. It is a derivative of acetamide, featuring a phenyl group at the 2-position and a phenylcarbamoyl group attached to the nitrogen atom. 2-phenyl-N-(phenylcarbamoyl)acetamide is characterized by its white crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is synthesized through the reaction of phenylacetamide with phenyl isocyanate, and it has potential applications in the pharmaceutical industry as a precursor for the synthesis of various drugs and medicinal compounds. The compound's chemical structure and properties make it a valuable intermediate in the development of new therapeutic agents.

4898-52-6

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4898-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4898-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,9 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4898-52:
(6*4)+(5*8)+(4*9)+(3*8)+(2*5)+(1*2)=136
136 % 10 = 6
So 4898-52-6 is a valid CAS Registry Number.

4898-52-6Downstream Products

4898-52-6Relevant academic research and scientific papers

Pd-Catalyzed Carbonylation of Acyl Azides

Chang, Wenxu,Fu, Bin,Huang, Baoliang,Jiao, Lei,Li, Zongyang,Wang, Peng,Xu, Shiyang,Yuan, Chenhui,Zhang, Zhenhua

, p. 9497 - 9508 (2019/08/26)

Pd-catalyzed reactions of azides with CO to access an isocynate intermediate have been developed extensively in recent years. However, the catalytic carbonylation of sensitive acyl azides has not been reported. Herein, we report a simple Pd-catalyzed carbonylation reaction of acyl azides with broad substrate scope, high efficiency, and simple operation under mild conditions, which provides facile access to acyl ureas. In addition, a mechanistic study was carried out by both experiment and DFT calculation. Control experiments and kinetic study revealed that the real active palladium species were Pd(0). The result of kinetic study suggested that palladium catalyst, azide, and CO were all involved in the turnover-limiting step except for amine. Further DFT study suggested that an unprecedented five-membered palladacycle intermediate was the key intermediate in the carbonylation reaction. ?

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