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2-acetyl-3-(4-bromo-anilino)-acrylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102148-04-9

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102148-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102148-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,4 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102148-04:
(8*1)+(7*0)+(6*2)+(5*1)+(4*4)+(3*8)+(2*0)+(1*4)=69
69 % 10 = 9
So 102148-04-9 is a valid CAS Registry Number.

102148-04-9Relevant academic research and scientific papers

Silver-Catalyzed Cross-Coupling of Isocyanides and Active Methylene Compounds by a Radical Process

Liu, Jianquan,Liu, Zhenhua,Liao, Peiqiu,Zhang, Lin,Tu, Tao,Bi, Xihe

supporting information, p. 10618 - 10622 (2015/09/02)

Isocyanides are versatile building blocks, and have been extensively exploited in C-H functionalization reactions. However, transition-metal-catalyzed direct C-H functionalization reactions with isocyanides suffer from over-insertion of isocyanides. Repor

N.M.R. Spectroscopical Investigations on 2-Acetyl-3-aminoacrylates

Michalik, M.

, p. 908 - 916 (2007/10/02)

The 2-acetyl-3-aminoacrylates 3 exist as Z/E-isomers, in which intramolecular H-bonds are formed between NH and acetyl or ester groups.The E-isomers are favoured due to the greater acceptor ability of the acetyl compared with ester group.In arylamino substituted compounds 3 a linear correlation with ?p constants have been found for 1H chemical shifts of CH and NH protons and for 13C chemical shifts of C-2 and C-3, respectively, representing an optimal transmission of substituent effects through the enamino system.The barriers of rotation around the C=C-bond of 3 h ave been determined by d n.m.r. spectroscopy.From coalescence phenomena the free activation enthalpies ΔG(excit.) of rotational process are determined and discussed with respect to substituent effects, a thermal rotational mechanism is postulated.

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