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2-Butenenitrile, 4-oxo-3,4-diphenyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64858-28-2

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64858-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64858-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,5 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64858-28:
(7*6)+(6*4)+(5*8)+(4*5)+(3*8)+(2*2)+(1*8)=162
162 % 10 = 2
So 64858-28-2 is a valid CAS Registry Number.

64858-28-2Downstream Products

64858-28-2Relevant academic research and scientific papers

Catalytic Direct Cyanomethylenation of C(sp3)–H Bonds via a One-Step Double C–C Bond Formation

Bhadra, Sukalyan,Kumar, Jogendra,Singh, Anupam Kumar

supporting information, p. 1512 - 1517 (2022/01/27)

An elegant and catalytic procedure for the one-step cyanomethylenation of C(sp3)–H bonds adjacent to benzazoles and ketones is described herein using DMF as a C-1 unit and TMSCN as the cyanide source. The copper-mediated reaction between DMF an

Highly efficient asymmetric hydrogenation of cyano-substituted acrylate esters for synthesis of chiral γ-lactams and amino acids

Kong, Duanyang,Li, Meina,Wang, Rui,Zi, Guofu,Hou, Guohua

, p. 1216 - 1220 (2016/02/03)

A highly efficient and enantioselective synthesis of γ-lactams and γ-amino acids by Rh-catalyzed asymmetric hydrogenation has been developed. Using the Rh-(S,S)-f-spiroPhos complex, under mild conditions a wide range of 3-cyano acrylate esters including both E and Z-isomers and β-cyano-α-aryl-α,β-unsaturated ketones were first hydrogenated with excellent enantioselectivities (up to 98% ee) and high turnover numbers (TON up to 10 000).

Nitrone cycloadditions to 1,2-diphenylcyclopropenes and subsequent transformations of the isoxazolidine cycloadducts

Diev, Vyacheslav V.,Stetsenko, Oksana N.,Tung, Tran Q.,Kopf, Juergen,Kostikov, Rafael R.,Molchanov, Alexander P.

, p. 2396 - 2399 (2008/09/18)

(Chemical Equation Presented) 1,3-Dipolar cycloaddition of C-aryl,N-aryl (or N-methyl) nitrones with a number of 1,2-diphenylcyclopropenes substituted at the C3 position occurs with the formation of expected "normal" cycloadducts (with N-methylnitrones) and products of their subsequent transformations. Among them are corresponding α-acetophenyl aziridines and tetra (or penta) -arylpyrroles. Aziridines and the normal cycloadducts can be also thermally converted to such arylpyrroles with moderate to good yields. Substitution at the C3 position of cyclopropenes by an electron acceptor group decreases the reactivity of cyclopropenes.

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