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614-25-5

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614-25-5 Usage

Chemical structure

A complex structure containing a benzene ring with two nitro groups (NNO-azoxy) attached to it.

Configuration

The compound features a 4-nitrophenyl group attached to the benzene ring in a Z configuration.

Usage

Industrial applications, such as dye intermediate, ingredient in the production of pharmaceuticals, and organic compounds.

Hazard classification

Classified as a hazardous chemical.

Health risks

Can pose health risks if proper safety measures are not followed.

Check Digit Verification of cas no

The CAS Registry Mumber 614-25-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 614-25:
(5*6)+(4*1)+(3*4)+(2*2)+(1*5)=55
55 % 10 = 5
So 614-25-5 is a valid CAS Registry Number.

614-25-5SDS

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 (4-nitrophenyl)-(4-nitrophenyl)imino-oxidoazanium

1.2 Other means of identification

Product number -
Other names 4,4'-dinitroazoxybenzene

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:614-25-5 SDS

614-25-5Relevant articles and documents

Efficient and Selective Oxidation of Aromatic Amines to Azoxy Derivatives over Aluminium and Gallium Oxide Catalysts with Nanorod Morphology

Singh, Bhawan,Mandelli, Dalmo,Pescarmona, Paolo P.

, p. 593 - 601 (2019/11/13)

Aluminium oxide and gallium oxide nanorods were identified as highly efficient heterogeneous catalysts for the selective oxidation of aromatic amines to azoxy compounds using hydrogen peroxide as environmentally friendly oxidant. This is the first report of the selective oxidation of aromatic amines to their azoxy derivatives without using transition metal catalysts. Among the tested transition-metal-free oxides, gallium oxide nanorods with small dimensions (9–52 nm length and 3–5 nm width) and fully accessible, high surface area (225 m2 g?1) displayed the best catalytic performance in terms of substrate versatility, activity and azoxybenzene selectivity. Furthermore, the catalyst loading, hydrogen peroxide type (aqueous or anhydrous), and the amount of solvent were tuned to optimise the catalytic performance, which allowed reaching almost full selectivity (98 %) towards azoxybenzene at high aniline conversion (94 %). Reusability tests showed that the gallium oxide nanorod catalyst can be recycled in consecutive runs with complete retention of the original activity and selectivity.

Nb2O5 supported on mixed oxides catalyzed oxidative and photochemical conversion of anilines to azoxybenzenes

De Carvalho, Gustavo Senra Gon?alves,Chagas, Luciano Honorato,Fonseca, Carla Grijó,De Castro, Pedro P?ssa,Sant'Ana, Ant?nio Carlos,Leit?o, Alexandre Amaral,Amarante, Giovanni Wilson

supporting information, p. 5863 - 5871 (2019/04/17)

The synthesis of novel supported niobium oxide catalysts and their application for aniline conversion to azoxybenzenes is described. The catalysts were successfully prepared by thermal decomposition of layered double hydroxides (LDHs), containing M2+ (M = Mg2+ and/or Zn2+) and Al3+ as layer cations, followed by niobium oxide incorporation employing the wetness impregnation method. These catalysts were fully characterized by both experimental techniques and theoretical calculations, and then successfully applied to the selective conversion of anilines into azoxybenzene derivatives, with up to 98% conversion and 92% isolated yield in the presence of violet light. Control experiments and DFT calculations revealed that the catalyst has a dual role in this transformation, acting both as a Lewis acid in the oxidative step and as a photocatalyst in the dimerization of the nitrosobenzene intermediate.

Aromatic amine oxidation process for preparing aromatic liquid discharge method

-

Paragraph 0014; 0015; 0016; 0017; 0018; 0019-0023; 0025, (2017/08/26)

The invention relates to a preparation method for aromatic-azoxybenzene by oxidizing aromatic amine. According to the method, air or oxygen is used as an oxygen source, and aromatic amine is oxidized to be aromatic-azoxybenzene under the effect of metal oxide catalyst. The method has the advantage of high product yield and is easy to separate the catalyst.

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