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1,3-Benzenediamine, N,N'-bis[4-(diphenylamino)phenyl]-N,N'-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

176243-72-4

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176243-72-4 Usage

Chemical compound

1,3-Benzenediamine, N,N'-bis[4-(diphenylamino)phenyl]-N,N'-diphenyl-

Physical appearance

Dark purple, powdery substance

Primary use

Dye intermediate in the production of various organic pigments and colorants

Solubility

High solubility in organic solvents, low solubility in water

Suitability

Suitable for solvent-based applications due to its solubility properties

Safety concerns

Potential to cause skin and eye irritation, requires caution when handling

Importance

Plays a significant role in the field of organic synthesis and colorant production

Check Digit Verification of cas no

The CAS Registry Mumber 176243-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,2,4 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 176243-72:
(8*1)+(7*7)+(6*6)+(5*2)+(4*4)+(3*3)+(2*7)+(1*2)=144
144 % 10 = 4
So 176243-72-4 is a valid CAS Registry Number.

176243-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,3-N-diphenyl-1-N,3-N-bis[4-(N-phenylanilino)phenyl]benzene-1,3-diamine

1.2 Other means of identification

Product number -
Other names -

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:176243-72-4 SDS

176243-72-4Downstream Products

176243-72-4Relevant academic research and scientific papers

Stable triplet-state di(cation radical)s of a N-phenylaniline oligomer

Wienk, Martijn M.,Janssen, Rene A. J.

, p. 267 - 268 (1996)

Two-electron oxidation of N,N′-bis[4-(diphenylamino)-phenyl]-N,N′-diphenyl-1,3-diaminobenzene produces a room temperature stable di(cation radical) with a triplet ground state as evidenced from EPR spectroscopy.

High-spin cation radicals of meta-para aniline oligomers

Wienk,Janssen

, p. 4492 - 4501 (2007/10/03)

A series of linear and branched high-spin di- and tri(cation radical)s (12.2+, 72.2+, 33.3+, 43.3+, and 93.3+) has been prepared by oxidation of the corresponding meta-para aniline oligomers. The oligo(cation radical)s are stable under ambient conditions. The formation and properties of the cation radicals has been studied in detail by cyclic voltammetry and UV-vis-near IR spectroscopy. ESR spectroscopy has provided the zero-field splittings, which are consistent with the topology of the molecules and the localization of the unpaired electrons. Variable temperature ESR measurements reveal that the signal intensity follows Curie's law, consistent with a low-energy high-spin state. The stability of the high- spin meta-para aniline oligomers and the possibility to extend these systems demonstrate that alternating meta and para aniline oligomers are promising building blocks for future polaronic ferromagnets.

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