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4792-83-0

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4792-83-0 Usage

Chemical Properties

orange-yellow to orange crystals or cryst. powder

Purification Methods

Crystallise the dye from toluene or EtOH. [Beilstein 16 II 326.]

Check Digit Verification of cas no

The CAS Registry Mumber 4792-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4792-83:
(6*4)+(5*7)+(4*9)+(3*2)+(2*8)+(1*3)=120
120 % 10 = 0
So 4792-83-0 is a valid CAS Registry Number.

4792-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-Azoxydiphenetole

1.2 Other means of identification

Product number -
Other names 4,4'-AZOXYDIPHENETOLE

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:4792-83-0 SDS

4792-83-0Relevant articles and documents

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Bogosslowsski

, (1937)

-

Method for synthesizing oxidized azo compound through selective oxidation of aromatic amine

-

Paragraph 0027-0051; 0052-0054; 0056, (2019/02/13)

The invention discloses a method for synthesizing an oxidized azo compound through selective oxidation of an aromatic amine, wherein an aromatic amine is used as a raw material, hydrogen peroxide is used as an oxidizing agent, a titanium-silicon molecular sieve or a metal modified titanium-silicon molecular sieve is used as a catalyst, and the aromatic amine is subjected to selective catalytic oxidation to prepare the corresponding oxidized azobenzene compound. According to the present invention, the method has advantages of environmental protection, good selectivity, high product yield, easyseparation and recycling of the catalyst, simple instrument required by the reaction, and easy operation.

Reduction of nitroarenes to azoxybenzenes by NaOH-PEG 400

Liu, Yufang,Liu, Bo,Guo, Ailing,Dong, Zhenming,Jin, Shuo,Lu, Yun

experimental part, p. 2201 - 2206 (2012/06/16)

The reduction of nitroarenes to azoxybenzenes by NaOH-PEG 400 in benzene is described. The protocol is facile, economical, and effective.

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