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1-(4-chlorophenyl)-2-(p-tolyl)diazene oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96294-55-2

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96294-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96294-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,9 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96294-55:
(7*9)+(6*6)+(5*2)+(4*9)+(3*4)+(2*5)+(1*5)=172
172 % 10 = 2
So 96294-55-2 is a valid CAS Registry Number.

96294-55-2Downstream Products

96294-55-2Relevant academic research and scientific papers

Synthesis of Unsymmetrical Aromatic Azoxy Compounds by Silver-Mediated Oxidative Coupling of Aromatic Amines with Nitrosoarenes

Ding, Weijie,Xu, Shengshi,Yu, Xiaochun,Wang, Shun

supporting information, (2019/02/07)

A silver(I) oxide-mediated synthesis of unsymmetrical aromatic azoxy compounds has been successfully achieved, wherein oxidative coupling reactions between aromatic amines and nitrosoarenes take place in ethanol under air. This reaction has very high economic value because silver(I) oxide is the only oxidant required and no other additive is needed. The resulted silver particles can be easily recovered, while the only other byproduct is water. This new procedure is compatible with various functional groups and proceeds under mild reaction conditions.

Perfluoroalkylation of azo compounds

Matsui, Masaki,Kawamura, Shigeo,Shibata, Katusoyoshi,Muramatsu, Hiroshige,Mitani, Motohiro,et al.

, p. 209 - 217 (2007/10/02)

Perfluoroalkyl azo dyes were prepared by the reaction of azo compounds with bis(perfluoroalkanoyl) peroxides.The absorption spectra and melting points of the perfluoroalkyl azo dyes were also examined.

Aryliminodimagnesium Reagents. XIV. Reactions with Nitrobenzenes Having Electronegative ortho-Substituents. Effects of Reaction Conditions on Condensation, Replacement, and Substitution

Okubo, Masao,Inatomi, Yoshito,Taniguchi, Naoki,Imamura, Kaori

, p. 3581 - 3586 (2007/10/02)

In reactions of ArN(MgBr)2 with o-MeO- and o-halo-substituted nitrobenzenes, types and yields of products were different from those in its reactions with m- and p-substituted substrates.Condensation (leading to unsymmetrical azoxy- and azobenzenes), o-substituent replacement, and nuclear substitution took place.Relative yields of products were greatly affected by substituents and reaction conditions. o-MeO and o-F favor replacement, while o-Cl, o-Br, and o-I favor substitution.Replacement and/or substitution predominate when small molar excess of reagent and low concentration are used, while condensation predominates when large molar excess of reagent and high concentration are used, which phenomenon is mechanistically discussed.

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