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N-(α-benzoylamino-cinnamoyl)-glycine ethyl ester is a complex organic compound with the molecular formula C20H19NO4. It is a derivative of glycine, an amino acid, and features a benzoylamino group attached to the α-carbon of a cinnamoyl moiety. N-(α-benzoylamino-cinnamoyl)-glycine ethyl ester is characterized by its ester functional group, which is an ethyl ester in this case. It is likely to be used in chemical research, particularly in the fields of pharmaceuticals or materials science, due to its unique structure that combines elements of both amino acids and esters. The compound's properties, such as its reactivity and potential applications, would be of interest to chemists studying the synthesis and behavior of complex organic molecules.

51012-69-2

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51012-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51012-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,1 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51012-69:
(7*5)+(6*1)+(5*0)+(4*1)+(3*2)+(2*6)+(1*9)=72
72 % 10 = 2
So 51012-69-2 is a valid CAS Registry Number.

51012-69-2Relevant academic research and scientific papers

A concise approach to polysubstituted oxazoles from N-acyl-2-bromo enamides via a copper(i)/amino acid-catalyzed intramolecular C-O bond formation

Liu, Bingjie,Zhang, Yueteng,Huang, Gang,Zhang, Xinting,Niu, Pengfei,Wu, Jie,Yu, Wenquan,Chang, Junbiao

, p. 3912 - 3923 (2014/06/09)

A straightforward and efficient copper(i)/amino acid-catalyzed intramolecular Ullmann-type C-O coupling reaction has been developed. This protocol affords a facile methodology for the synthesis of a series of novel 2,4,5-substituted oxazoles from readily accessible N-acyl-2-bromo enamides under mild conditions. This journal is the Partner Organisations 2014.

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