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3,7-bis(perfluorophenyl)benzo[1,2-b:4,5-b']difuran-2,6-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1400280-34-3

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1400280-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1400280-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,0,2,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1400280-34:
(9*1)+(8*4)+(7*0)+(6*0)+(5*2)+(4*8)+(3*0)+(2*3)+(1*4)=93
93 % 10 = 3
So 1400280-34-3 is a valid CAS Registry Number.

1400280-34-3Relevant academic research and scientific papers

Toward Sustainable Organic Semiconductors from a Broad Palette of Green Reactions

Faurie, Alexandre,Grolleau, Jérémie,Gohier, Frédéric,Allain, Magali,Legoupy, Stéphanie,Frère, Pierre

, p. 2707 - 2714 (2017)

New conjugated materials, based on the triphenylamine-thiophene moiety and integrating azomethine bonds with a dibenzofuran unit or a cyanovinyl bond with a phenylthiophene or bithiophene unit, have been synthesized by using a wide range of green reaction

Preponderant role of pentafluorophenyl moieties for tuning the electronic properties of extended benzodifuran-azomethine derivatives

Moussallem, Chady,Allain, Magali,Gohier, Frédéric,Frère, Pierre

, p. 8647 - 8653 (2021)

From a central 3,7-bis(perfluorophenyl)-BDF unit, the extension performed with electron acceptor perfluorophenyl groups and/or electron donor N,N-dimethylamino groups via an imine link leads to symmetrical AAA and DAD or dissymmetrical DA materials. X-Ray solid state structures were also studied, revealing a strong involvement of the perfluorinated phenyl group in the arrangement. The two symmetrical derivatives show emission properties in solvents which are quenched in the solid state whereas the DA derivative shows opposite behavior with Aggregation Induced Emission (AIE) properties.

Extended benzodifuran-thiophene systems connected with azomethine junctions: Synthesis and electronic properties

Moussallem, Chady,Gohier, Frédéric,Frère, Pierre

, p. 5116 - 5119 (2015)

The synthesis of extended benzodifuran-thiophene systems connected by azomethine junctions is described. The electronic properties of these systems, studied by UV-vis spectroscopy and cyclic voltammetry, are discussed in relation with the electron withdra

Extended benzodifuran-furan derivatives as example of π-conjugated materials obtained from sustainable approach

Moussallem, Chady,Gohier, Frédéric,Mallet, Charlotte,Allain, Magali,Frre, Pierre

, p. 8617 - 8621 (2012/10/29)

The synthesis of extended benzodifuran-furan systems are described as an example of π-conjugated materials prepared by following a green approach with only water being produced as waste and using furan derivatives from renewable sources. Investigation of their optical and electrochemical properties shows that the new compounds present electronic properties compatible for application in organic electronics.

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