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2-ethanoly-4-nitro-N-phenylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79110-06-8

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79110-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79110-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79110-06:
(7*7)+(6*9)+(5*1)+(4*1)+(3*0)+(2*0)+(1*6)=118
118 % 10 = 8
So 79110-06-8 is a valid CAS Registry Number.

79110-06-8Downstream Products

79110-06-8Relevant academic research and scientific papers

Synthesis of functionalized 4-nitroanilines by ring transformation of dinitropyridone with enaminones

Naito, Saki,Yokoyama, Soichi,Asahara, Haruyasu,Nishiwaki, Nagatoshi

, p. 4699 - 4702 (2017)

2-Functionalized 4-nitroanilines were readily synthesized by ring transformation using 3,5-dinitro-2-pyridone and enaminones prepared from 1,3-dicarbonyl compounds and amines. Modification of the amino group and the ortho-position could be achieved by sim

The Preparation of Some 2-Nitroacridines and Related Compounds

Rosevear, Judi,Wilshire, John F. K.

, p. 839 - 853 (2007/10/02)

The reaction of 2-fluoro-5-nitrobenzaldehyde with a wide variety of arylamines gives, in general, mixtures of the corresponding 2-arylamino-5-nitrobenzaldehydes and their related anils.Both aldehydes and anils readily underwent acid-catalysed cyclization to give the corresponding 2-nitroacridines.The effect of substituent on the rate of cyclization of these aldehydes and of some related anilino-benzaldehydes and -acetophenones has been studied in trifluoroacetic acid solution by means of 1H n.m.r. spectroscopy.A solution of 2-(N-methylanilino)-5-nitrobenzaldehydein trifluoroacetic acid appears to contain a substituted acridinium ion; treatment of this solution with alkali gave 10-methyl-2-nitroacridone. 1H n.m.r. data for a wide variety of substituted 2-nitroacridines are discussed.

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