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1,4-Benzenediamine, N-[4-[(4-aminophenyl)imino]-2,5-cyclohexadien-1-ylidene]-N'-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2908-00-1

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2908-00-1 Usage

Chemical class

Aromatic amine

Molecular structure

Complex, with multiple nitrogen atoms and aromatic rings

Industrial applications

Production of dyes, polymers, and pharmaceuticals

Chemical properties

Strong reducing agent

Reactivity

Can react with oxidizing agents

Health hazards

Poses health risks if not handled properly

Safety measures

Important to handle with care and ensure proper safety measures are in place

Potential mutagenic properties

Known to have potential mutagenic properties

Potential carcinogenic properties

Known to have potential carcinogenic properties

Check Digit Verification of cas no

The CAS Registry Mumber 2908-00-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2908-00:
(6*2)+(5*9)+(4*0)+(3*8)+(2*0)+(1*0)=81
81 % 10 = 1
So 2908-00-1 is a valid CAS Registry Number.

2908-00-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name amine/phenyl-capped tetraaniline

1.2 Other means of identification

Product number -
Other names [1,4]Benzochinon-(4-amino-phenylimin)-(4-anilino-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:2908-00-1 SDS

2908-00-1Relevant academic research and scientific papers

A robust pathway to electrically conductive hemicellulose hydrogels with high and controllable swelling behavior

Zhao, Weifeng,Glavas, Lidija,Odelius, Karin,Edlund, Ulrica,Albertsson, Ann-Christine

, p. 2967 - 2976 (2014)

A robust pathway to synthesize electrically conductive hemicellulose hydrogels (ECHHs) based on O-acetyl-galactoglucomannan (AcGGM) and conductive aniline tetramer (AT) is presented. These ECHHs were obtained by functionalizing carboxylated AcGGM with gly

Degradable and electroactive hydrogels with tunable electrical conductivity and swelling behavior

Guo, Baolin,Finne-Wistrand, Anna,Albertsson, Ann-Christine

, p. 1254 - 1262 (2011)

Degradable electrically conducting hydrogels (DECHs), which combine the unique properties of degradable polymers and electrically conducting hydrogels, were synthesized by introducing biodegradable segments into conductive hydrogels. These DECHs were obta

Morphological and dimensional control via hierarchical assembly of doped oligoaniline single crystals

Wang, Yue,Liu, Jinglin,Tran, Henry D.,Mecklenburg, Matthew,Guan, Xin N.,Stieg, Adam Z.,Regan,Martin, David C.,Kaner, Richard B.

, p. 9251 - 9262 (2012)

Single crystals of doped aniline oligomers are produced via a simple solution-based self-assembly method. Detailed mechanistic studies reveal that crystals of different morphologies and dimensions can be produced by a "bottom-up" hierarchical assembly whe

Nanoscale morphology, dimensional control, and electrical properties of oligoanilines

Wang, Yue,Tran, Henry D.,Liao, Lei,Duan, Xiangfeng,Kaner, Richard B.

experimental part, p. 10365 - 10373 (2010/09/06)

While nanostructures of organic conductors have generated great interest in recent years, their nanoscale size and shape control remains a significant challenge. Here, we report a general method for producing a variety of oligoaniline nanostructures with well-defined morphologies and dimensionalities. 1-D nanowires, 2-D nanoribbons, and 3-D rectangular nanoplates and nanoflowers of tetraaniline are produced by a solvent exchange process in which the dopant acid can be used to tune the oligomer morphology. The process appears to be a general route for producing nanostructures for a variety of other aniline oligomers such as the phenyl-capped tetramer. X-ray diffraction of the tetraniline nanostructures reveals that they possess different packing arrangements, which results in different nanoscale morphologies with different electrical properties for the structures. The conductivity of a single tetraaniline nanostructure is up to 2 orders of magnitude higher than the highest previously reported value and rivals that of pressed pellets of conventional polyaniline doped with acid. Furthermore, these oligomer nanostructures can be easily processed by a number of methods in order to create thin films composed of aligned nanostructures over a macroscopic area.

Synthesis and spectroscopic properties of aniline tetramers. Comparative studies

Kulszewicz-Bajer, Irena,Rozalska, Izabela,Kurylek, Malgorzata

, p. 669 - 675 (2007/10/03)

A new synthetic method involving SNAr coupling of 4-fluoronitrobenzene to arylamines, followed by the reduction of the nitro groups, has been developed. Two types of aniline oligomers, namely Ph/NH 2 and NH2/NH2

Synthesis of starburst hexa(oligoanilinated) C60 using hexanitro[60]fullerene as a precursor

Anantharaj, Vijayaraj,Wang, Lee Y.,Canteenwala, Taizoon,Chiang, Long Y.

, p. 3357 - 3366 (2007/10/03)

Efficient syntheses of starburst hexaanilino, hexa(dianilino), hexa(tetraanilino), and hexa(hexadecaanilino)-[60]fullerenes (HHDAF) were demonstrated using hexanitro[60]fullerene (HNF) as a reactive precursor molecule. The tertiary nitro groups of HNF wer

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