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(Z)-2-cyano-3-phenylbut-2-enamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25327-41-7

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25327-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25327-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,2 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25327-41:
(7*2)+(6*5)+(5*3)+(4*2)+(3*7)+(2*4)+(1*1)=97
97 % 10 = 7
So 25327-41-7 is a valid CAS Registry Number.

25327-41-7Downstream Products

25327-41-7Relevant academic research and scientific papers

Homogeneous and stereoselective copper(II)-catalyzed monohydration of methylenemalononitriles to 2-cyanoacrylamides

Xin, Xiaoqing,Xiang, Dexuan,Yang, Jiming,Zhang, Qian,Zhou, Fenguo,Dong, Dewen

, p. 11956 - 11961 (2014/01/06)

A facile and efficient route for the homogeneous and highly stereoselective monohydration of substituted methylenemalononitriles to (E)-2-cyanoacrylamides catalyzed by copper(II) acetate monohydrate in acetic acid containing 2% water is described, and a mechanism is proposed. The protocol has proved to be suitable for the monohydration of dicyanobenzenes and 2-substituted malononitriles.

Titanium isopropoxide/pyridine mediated Knoevenagel reactions

Robichaud, Brian A.,Liu, Kevin G.

experimental part, p. 6935 - 6938 (2012/02/05)

We report a Ti(OiPr)4/pyridine-mediated Knoevenagel reaction between aromatic ketones and cyanoacetamides to provide Knoevenagel olefin products in good to excellent yields. Almost in all cases studied, a single geometrical isomer was formed an

Arylcyanoacrylamides as inhibitors of the Dengue and West Nile virus proteases

Nitsche, Christoph,Steuer, Christian,Klein, Christian D.

experimental part, p. 7318 - 7337 (2012/01/05)

The 3-aryl-2-cyanoacrylamide scaffold was designed as core pharmacophore for inhibitors of the Dengue and West Nile virus serine proteases (NS2B-NS3). A total of 86 analogs was prepared to study the structure-activity relationships in detail. Thereby, it turned out that the electron density of the aryl moiety and the central double bond have a crucial influence on the activity of the compounds, whereas the influence of substituents of the amide residue is less relevant. The para-hydroxy substituted analog was found to be the most potent inhibitor in this series with a Ki-value of 35.7 μM at the Dengue and 44.6 μM at the West Nile virus protease. The aprotinin competition assay demonstrates a direct interaction of the inhibitor molecule with active centre of the Dengue virus protease. The target selectivity was studied in a counterscreen with thrombin and found to be 2.8:1 in favor of DEN protease and 2.3:1 in favor of WNV protease, respectively.

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