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Diazene, (2-methylphenyl)phenyl-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34810-71-4

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34810-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34810-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,1 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34810-71:
(7*3)+(6*4)+(5*8)+(4*1)+(3*0)+(2*7)+(1*1)=104
104 % 10 = 4
So 34810-71-4 is a valid CAS Registry Number.

34810-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-N'-o-tolyl-diazene-N-oxide

1.2 Other means of identification

Product number -
Other names 2-Methylazoxybenzol

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:34810-71-4 SDS

34810-71-4Relevant academic research and scientific papers

Synthesis of Unsymmetrical Azoxyarenes via Copper-Catalyzed Aerobic Oxidative Dehydrogenative Coupling of Anilines with Nitrosoarenes

Shi, Chongyang,Xu, Boxia,Fang, Xiaolan,Yu, Xiaochun,Jin, Huile,Wang, Shun

supporting information, p. 1963 - 1967 (2021/03/04)

A copper-catalyzed oxidative dehydrogenative coupling of nitrosobenzenes with anilines for the synthesis of unsymmetrical azoxybenzenes was developed. This approach uses O2 as the oxidant. The reaction products are diverse unsymmetrical azoxybe

Efficient synthesis of 2-aryl-2: H -indazoles by base-catalyzed benzyl C-H deprotonation and cyclization

Gao, Wen-Xia,Jin, Guo-Qing,Liu, Miao-Chang,Wu, Hua-Yue,Zhou, Yun-Bing

supporting information, p. 14617 - 14620 (2020/12/02)

A straightforward and efficient method for the preparation of 2-aryl-2H-indazoles from ortho-alkyl substituted azoxybenzenes is presented. The reaction proceeds through base-catalyzed benzyl C-H deprotonation and cyclization to afford 2-aryl-2H-indazoles

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.

Synthesis method of asymmetric azoxybenzene compound

-

Paragraph 0071-0073, (2018/11/04)

The invention relates to a synthesis method of an asymmetric azoxybenzene compound. According to the synthesis method, in an organic solvent, silver oxide is taken as the only promoter to carry out dehydrogenation condensation reactions. According to the

Synthesis method of asymmetric azoxybenzene compound

-

Paragraph 0047; 0048; 0049, (2018/09/08)

The invention relates to a synthesis method of an asymmetric azoxybenzene compound. According to the method, in an organic solvent, a compound system comprising iodine and an auxiliary ensures that anaromatic ammonia compound and a nitrosobenzene compound react, and a series of asymmetric azoxybenzene is specifically obtained. The method is simple in reaction, simple to operate, good in selectivity and high in yield, belongs to a new synthesis method of the asymmetric azoxybenzene compound, provides a novel synthesis route for the preparation of the compound, and has excellent scientific research value and industrial potential.

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