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9,14-Diphenyldibenzoanthracene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77079-17-5

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77079-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77079-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,7 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77079-17:
(7*7)+(6*7)+(5*0)+(4*7)+(3*9)+(2*1)+(1*7)=155
155 % 10 = 5
So 77079-17-5 is a valid CAS Registry Number.

77079-17-5Relevant academic research and scientific papers

A Comprehensive Study of Isoskeletal Analogs of Dibenzoanthracene

Dias, Jerry R.,Liu, Binglan

, p. 13 - 30 (1990)

While reviewing the chemistry of cyclopentadienone derivatives and aza isoskeletal analogs of dibenzoanthracene, additional molecular orbital (MO) and spectroscopic results and insights are presented.The MO tendency for coplanarity of phenyl substitu

Fluorinated Phenanthrenes as Aryne Precursors: PAH Synthesis Based on Domino Ring Assembly Using 1,1-Difluoroallenes

Abe, Masashi,Fuchibe, Kohei,Ichikawa, Junji,Idate, Hiroto

, (2020/03/05)

On treatment with the catalyst InBr3, 1,1-difluoroallenes that bear a cyclopentene moiety and an aryl group underwent domino ring assembly in the presence or absence of N-bromosuccinimide or N-iodosuccinimide to afford aryne precursors such as three-ringed ortho-fluoro(halo)phenanthrenes, four-ringed ortho-fluoro(halo)tetraphenes, ortho-fluoro(halo)chrysenes and fluoro[4]helicenes. Metalation of the aryne precursors followed by elimination of the fluoride resulted in the unprecedented systematic generation of arynes bearing π-extended systems. Diels?Alder reactions of these arynes with isobenzofurans afforded the corresponding cycloadducts whose reductive aromatisation in an SnCl2/HBr system furnished fully aromatised benzotriphenylenes. In addition, oxidative aryl?aryl coupling (the Scholl reaction) of these benzotriphenylenes facilitated the synthesis of ‘half HBCs’ (hexabenzocoronenes).

DIBENZOANTHRACENE COMPOUND AND ORGANIC LIGHT EMITTING DEVICE HAVING THE SAME

-

Page/Page column 16-17, (2008/06/13)

Provided is a novel dibenzo [a, c] anthracene compound having substituents represented by the following structural formula (I), which can be used in an organic light emitting device.

Reaction of phencyclone with aryne and bisaryne

Mallakpour, Shadpour E.,Karami-Dezcho, Bahador

, p. 552 - 556 (2007/10/03)

Benzyne (2a) and 4-chlorobenzyne (2b) from the corresponding anthranilic acids have been reacted with 1,3-diphenyl-2H-cyclopent[b]phenanthren-2-one (3) (phencyclone) at different temperature. In boiling 1,2-dichloroethane, a mixture of carbonyl-bridged ad

A Study of Substituent Effects on Hydrogen-to-Arene Nonbonded Interactions

L'Esperance, Robert P.,Engen, Donna Van,Dayal, Rajeev,Pascal, Robert A.

, p. 688 - 694 (2007/10/02)

The polycyclic aromatic hydrocarbon 9,14-diphenylbenzotriphenylene is strongly twisted due to nonbonded interactions between hydrogen atoms on the polycyclic nucleus and the ? systems of the phenyl groups.Ten derivatives of 9,14-diphenylbenzotriphen

Polycyclic Aromatic Compounds: Part VIII - A New Synthesis of Polycyclics Containing Phenanthrene Nucleus

Mondal, S.,Bandyopadhyay, T. K.,Bhattacharya, A. J.

, p. 448 - 452 (2007/10/02)

A new series of polycyclic aromatic compounds with phenanthrene nucleus have been prepared.The method involves Diels Alder cycloaddition reaction of 1,3-diaryl-2H-cyclopentaphenanthren-2-one (I) with various dienophiles, viz. bicyclohepta-2,5-di

Synthesen, ESR- und ENDOR-Untersuchungen hochverdrillter phenylsubstituierter Radikalanionen

Grein, Kornelia,Kirste, Burkhard,Kurreck, Harry

, p. 254 - 266 (2007/10/02)

The synthesis of a variety of phenyl substituted and partially deuterated derivatives of anthracene, naphthalene, benzotriphenylene, and benzofluoranthene is given.By performing ESR, ENDOR, and TRIPLE experiments the hyperfine coupling constants, in

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