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N,N'-Diphenyl-2,5-bis(phenylamino)-1,4-benzoquinone diimine is a complex organic compound with the chemical formula C36H26N2O2. It is characterized by a 1,4-benzoquinone core, which is a type of quinone, with two phenylamino groups attached at the 2 and 5 positions. Additionally, it has two phenyl groups attached to the nitrogen atoms, which are part of the diimine structure. N,N'-Diphenyl-2,5-bis(phenylamino)-1,4-benzoquinone diimine is known for its potential applications in the field of materials science, particularly in the development of organic electronics and as a precursor in the synthesis of other complex molecules. Its structure provides it with unique electronic properties, making it a subject of interest for researchers exploring novel materials with specific functionalities.

4435-12-5

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4435-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4435-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4435-12:
(6*4)+(5*4)+(4*3)+(3*5)+(2*1)+(1*2)=75
75 % 10 = 5
So 4435-12-5 is a valid CAS Registry Number.

4435-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,4-N-diphenyl-3,6-bis(phenylimino)cyclohexa-1,4-diene-1,4-diamine

1.2 Other means of identification

Product number -
Other names 2,5-Dianilino-[1,4]benzochinon-bis-phenylimin

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:4435-12-5 SDS

4435-12-5Relevant academic research and scientific papers

An azophenine radical-bridged Fe2 single-molecule magnet with record magnetic exchange coupling

Jeon, Ie-Rang,Park, Jesse G.,Xiao, Dianne J.,Harris, T. David

, p. 16845 - 16848 (2013)

One-electron reduction of the complex [(TPyA)2Fe II2(NPhL2-)]2+ (TPyA = tris(2-pyridylmethyl)amine, NPhLH2 = azophenine = N,N′,N″,Na€-tetraphenyl-2,5-diamino-1, 4-diim

NMR Study of Kinetic HH/HD/DD Isotope, Solvent, and Solid-State Effects on the Double Proton Transfer in Azophenine

Rumpel, Helmut,Limbach, Hans-Heinrich

, p. 5429 - 5441 (2007/10/02)

Azophenine (AP, N,N'-diphenyl-3,6-bis(phenylimino)-1,4-cyclohexadiene-1,4-diamine) is subject in liquid solution to a fast intramolecular double proton transfer involving two degenerate tautomers.Rate constants of this reaction have been measured as a fun

THERMAL AND PHOTOCHEMICAL DECOMPOSITION OF 3- AND 4-AZIDOPYRIDINE 1-OXIDES IN NUCLEOPHILIC SOLVENTS

Abramovitch, Rudolph A.,Bachowska, Barbara,Tomasik, Piotr

, p. 805 - 815 (2007/10/02)

The thermolysis and photolysis of the title compounds in aniline, N-methylaniline, N,N-dimethylaniline, morpholine and dioxane containing methoxide ion in methanol afforded complex mixtures from which only major products were isolated.No ring-expansion products were detected.In aniline, many of its known oxidation products were found, the N-oxide acting as an oxidizing agent.Hydrogen-abstraction products were the main ones formed from pyridine 1-oxides.

A Novel Synthesis of Azophenines

Merchant, J. R.,Martyres, Gail,Shinde, N. M.

, p. 1405 - 1406 (2007/10/02)

Arylamines react with polyhaloalkanes in the presence of copper bronze to yield azophenines.

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