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Benzenepropanenitrile, b-oxo-a-[(phenylamino)methylene]-, also known as 3-phenyl-2-cyanoacrylamide, is an organic compound with the chemical formula C10H8N2O. It is a derivative of benzenepropanenitrile, featuring a cyano group (-CN) at the 2-position and a phenyl group (C6H5) attached to the 3-position. The molecule also contains an amide group (-CONH2) and a carbonyl group (C=O) at the 1-position. Benzenepropanenitrile, b-oxo-a-[(phenylamino)methylene]- is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other chemical products.

6123-64-4

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6123-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6123-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6123-64:
(6*6)+(5*1)+(4*2)+(3*3)+(2*6)+(1*4)=74
74 % 10 = 4
So 6123-64-4 is a valid CAS Registry Number.

6123-64-4Relevant academic research and scientific papers

Microwave-assisted synthesis of 5-aminopyrazol-4-yl ketones and the p38MAPK inhibitor RO3201195 for study in Werner syndrome cells

Bagley, Mark C.,Davis, Terence,Dix, Matthew C.,Murziani, Paola G.S.,Rokicki, Michal J.,Kipling, David

scheme or table, p. 3745 - 3748 (2009/04/04)

5-Aminopyrazol-4-yl ketones are prepared rapidly and efficiently using microwave dielectric heating from β-ketonitriles by treatment with N,N′-diphenylformamidine followed by heterocyclocondensation by irradiation with a hydrazine. The inhibitory activity of RO3201195 prepared by this methodology was confirmed in hTERT-immortalized HCA2 and WS dermal fibroblasts at 200 nM concentration, both by ELISA and immunoblot assay, and displays excellent kinase selectivity for p38α MAPK over the related stress-activated kinase JNK.

β,β-Diacyl-enamine und -enole, 9. Zur Darstellung von Aminomethylenderivaten offenkettiger CH2-acider Verbindungen

Wolfbeis, Otto S.

, p. 3471 - 3484 (2007/10/02)

The reaction of a combination of primary or secondary aromatic or aliphatic amines with orthocarboxylic esters upon a variety of open-chain CH2-acidic molecules gives N-substituted aminoalkylidene derivatives.The method is highly recommended for methylene

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