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α-Formylamino-β-phenyl-zimtsaeure-ethylester, also known as ethyl α-formylamino-β-phenyl cinnamate, is a chemical compound with the molecular formula C16H15NO3. It is a derivative of cinnamic acid, featuring an ethyl ester group, a phenyl ring, and a formylamino group. α-Formylamino-β-phenyl-zimtsaeure-ethylester is characterized by its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure. It is an important intermediate in the preparation of certain drugs and can also be used in the development of novel chemical entities with potential therapeutic properties. The compound's structure allows for further functionalization and modification, making it a versatile building block in organic synthesis.

25315-41-7

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25315-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25315-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,1 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25315-41:
(7*2)+(6*5)+(5*3)+(4*1)+(3*5)+(2*4)+(1*1)=87
87 % 10 = 7
So 25315-41-7 is a valid CAS Registry Number.

25315-41-7Relevant academic research and scientific papers

Silver-catalyzed oxidative decarboxylation of difluoroacetates: Efficient access to C-CF2 bond formation

Wan, Wen,Ma, Guobin,Li, Jialiang,Chen, Yunrong,Hu, Qingyang,Li, Minjie,Jiang, Haizhen,Deng, Hongmei,Hao, Jian

, p. 1598 - 1601 (2016)

A mild, versatile and efficient method for the silver(i)-catalyzed oxidative decarboxylative gem-difluoromethylenation has been developed. The radical cascade reaction comprises the addition of an oxidatively generated difluoromethylene radical to the isonitrile functionality and subsequent homolytic aromatic substitution. It provides a novel and efficient access to the C-CF2 bond formation.

4CzIPN-tBu-Catalyzed Proton-Coupled Electron Transfer for Photosynthesis of Phosphorylated N-Heteroaromatics

Liu, Yan,Chen, Xiao-Lan,Li, Xiao-Yun,Zhu, Shan-Shan,Li, Shi-Jun,Song, Yan,Qu, Ling-Bo,Yu, Bing

supporting information, p. 964 - 972 (2021/01/12)

2,4,5,6-Tetrakis(3,6-di-tert-butyl-9H-carbazol-9-yl)isophthalonitrile (4CzIPN-tBu) was developed as a photocatalyst for the phosphorus-radical-initiated cascade cyclization reaction of isocyanides. By using 4CzIPN-tBu as catalyst, we developed a visible-light-induced proton-coupled electron transfer strategy for the generation of phosphorus-centered radicals, via which a wide range of phosphorylated phenanthridines, quinolines, and benzothiazoles were successfully constructed.

Metal-Free Radical Cyclization of Vinyl Isocyanides with Alkanes: Synthesis of 1-Alkylisoquinolines

Xue, Dengqi,Xue, Yijie,Yu, Haihua,Shao, Liming

supporting information, p. 874 - 884 (2019/02/10)

A metal-free radical cyclization reaction of vinyl isocyanides with alkanes is developed, allowing convenient access to a diverse range of potentially valuable 1-alkylisoquinolines. The methodology is simple and efficient, demonstrating excellent functional group tolerance and broad substrate scope. A mechanism involving a radical process is supported by kinetic isotope effect and radical inhibition studies.

Mn(ii)/O2-promoted oxidative annulation of vinyl isocyanides with boronic acids: Synthesis of multi-substituted isoquinolines

Wang, Hao,Yu, Yang,Hong, Xiaohu,Xu, Bin

supporting information, p. 13485 - 13488 (2015/01/16)

An efficient manganese(ii)/O2-promoted oxidative radical cascade reaction was developed for the modular synthesis of multi-substituted isoquinolines from easily accessible vinyl isocyanides and boronic acids.

1-Trifluoromethylated isoquinolines via radical trifluoromethylation of isonitriles

Zhang, Bo,Studer, Armido

supporting information, p. 9895 - 9898 (2015/01/08)

A simple and efficient approach to biologically important 1-trifluoromethylated isoquinolines starting with readily prepared β-aryl-α-isocyano-acrylates and the commercially available Togni reagent as the CF3 radical precursor is described. The

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