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Benzamide, N-[(butylamino)carbonyl]-, also known as N-(butylcarbamoyl)benzamide, is an organic compound with the chemical formula C11H14N2O2. It is a white crystalline solid that is soluble in water and various organic solvents. Benzamide, N-[(butylamino)carbonyl]- is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other chemical products. It is synthesized through the reaction of benzoic acid with butyl isocyanate, followed by the formation of the amide group. Due to its potential applications in the development of new drugs and chemicals, it has gained significant attention in the field of organic chemistry and pharmaceutical research.

3576-28-1

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3576-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3576-28-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3576-28:
(6*3)+(5*5)+(4*7)+(3*6)+(2*2)+(1*8)=101
101 % 10 = 1
So 3576-28-1 is a valid CAS Registry Number.

3576-28-1Downstream Products

3576-28-1Relevant 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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