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Diazene, (3-methoxyphenyl)phenyl-, (1E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56058-94-7

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56058-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56058-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,5 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56058-94:
(7*5)+(6*6)+(5*0)+(4*5)+(3*8)+(2*9)+(1*4)=137
137 % 10 = 7
So 56058-94-7 is a valid CAS Registry Number.

56058-94-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methoxyphenyl)-phenyldiazene

1.2 Other means of identification

Product number -
Other names 3-Methoxy-trans-azobenzol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56058-94-7 SDS

56058-94-7Relevant academic research and scientific papers

Chemoselective Hydrogenation of Nitroarenes Using an Air-Stable Base-Metal Catalyst

Zubar, Viktoriia,Dewanji, Abhishek,Rueping, Magnus

supporting information, p. 2742 - 2747 (2021/05/05)

The reduction of nitroarenes to anilines as well as azobenzenes to hydrazobenzenes using a single base-metal catalyst is reported. The hydrogenation reactions are performed with an air-and moisture-stable manganese catalyst and proceed under relatively mild reaction conditions. The transformation tolerates a broad range of functional groups, affording aniline derivatives and hydrazobenzenes in high yields. Mechanistic studies suggest that the reaction proceeds via a bifunctional activation involving metal-ligand cooperative catalysis.

Palladium-catalyzed direct ortho-sulfonylation of azobenzenes with arylsulfonyl chlorides via C-H activation

Xia, Chengcai,Wei, Zhenjiang,Shen, Chao,Xu, Jun,Yang, Yong,Su, Weike,Zhang, Pengfei

, p. 52588 - 52594 (2015/06/25)

A highly efficient and practical procedure to direct ortho-sulfonylation of azobenzenes' C-H bond with arylsulfonyl chlorides has been developed. The method was applicable to both electron-rich and electron-deficient substrates and delivered good yields f

One step synthesis of azo compounds from nitroaromatics and anilines

Zhao, Rui,Tan, Chunyan,Xie, Yonghua,Gao, Chunmei,Liu, Hongxia,Jiang, Yuyang

supporting information; experimental part, p. 3805 - 3809 (2011/08/09)

A general and efficient method for synthesis of both symmetric and asymmetric aromatic azo compounds in one single step has been developed. The nitro compounds were reduced and the substituted anilines were oxidized by each other without any metal in the

Reactions of dry arenediazonium o-benzenedisulfonimides with triorganoindium compounds

Barbero, Margherita,Cadamuro, Silvano,Dughera, Stefano,Giaveno, Cinzia

, p. 4884 - 4890 (2007/10/03)

The reaction between various arenediazonium o-benzenedisulfonimides and triorganoindium compounds is described. Depending on the reaction conditions, it is possible to obtain biaryls (16 examples, average yield of 79%) or diaryldiazenes (18 examples, average yield of 81 %). o-Benzenedisulfonimide can be recovered and reused to prepare additional arenediazonium o-benzenedisulfonimides. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Preparation of diazenes by electrophile C-coupling reactions of dry arenediazonium o-benzenedisulfonimides with Grignard reagents

Barbero, Margherita,Degani, Iacopo,Dughera, Stefano,Fochi, Rita,Perracino, Paolo

, p. 1235 - 1237 (2007/10/03)

The diaryldiazenes (19 examples) and aryl(tertbutyl)diazenes (3 examples) 3 were prepared by electrophilic C-coupling reactions of dry arenediazonium o-benzenedisulfonimides 1 with Grignard reagents. The reactions were carried out in anhyd THF at -78°C un

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