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7,9-bis-(4-methoxyphenyl)-8H-cyclopenta[a]acenaphthylen-8-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86997-94-6

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86997-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86997-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,9 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86997-94:
(7*8)+(6*6)+(5*9)+(4*9)+(3*7)+(2*9)+(1*4)=216
216 % 10 = 6
So 86997-94-6 is a valid CAS Registry Number.

86997-94-6Relevant academic research and scientific papers

ORGANIC COMPOUND, ORGANIC LIGHT EMITTING DIODE AND ORGANIC LIGHT EMITTING DEVICE INCLUDING THE ORGANIC COMPOUND

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Paragraph 0250-0254, (2021/03/11)

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. Incorporating the organic compound into an emissive layer

ORGANIC COMPOUND, ORGANIC LIGHT EMITTING DIODE AND ORGANIC LIGHT EMITTING DEVICE INCLUDING THE ORGANIC COMPOUND

-

Paragraph 0217-0218, (2021/03/13)

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. Applying the organic compound into an emissive layer make

Diels-alder reaction of isobenzofurans/cyclopentadienones with tetrathiafulvalene: Preparation of naphthalene, fluoranthene, and fluorenone derivatives

Karunakaran, Jayachandran,Mohanakrishnan, Arasambattu K.

supporting information, p. 966 - 970 (2018/02/23)

Diels-Alder reaction of 1,3-diarylbenzo[c]furan/cyclopentadienone with TTF followed by triflic acid mediated cleavage of the resulting adducts led to the formation of the respective 1,4-diaryl substituted naphthalenes, fluoranthenes, and fluorenones. The photophysical properties of representative diaryl-substituted hydrocarbons are also reported.

Alkylene-chain effect on microwire growth and crystal packing of π-moieties

Ding, Lin,Li, Hai-Bin,Lei, Ting,Ying, Han-Ze,Wang, Rui-Bo,Zhou, Yan,Su, Zhong-Min,Pei, Jian

scheme or table, p. 1944 - 1949 (2012/08/13)

We developed a facile approach to modulate molecular arrangement through dimerizing of π-moieties and tuning alkylene-bridge length. Dimers of fluoranthene-fused imide (DFAI-Cns) with various lengths of alkylene chains were synthesized by a Diels-Alder re

Efficient synthesis of substituted polyarylphthalimides via cycloaddition of cyclopentadienones with 2-bromomaleimide

Vanel, Rémi,Berthiol, Florian,Bessières, Bernard,Einhorn, Cathy,Einhorn, Jacques

, p. 1293 - 1295 (2011/07/07)

Functionalized tetraarylphthalimides or diarylphthalimides fused with an acenaphthene moiety have been prepared in one step from 2-bromomaleimide and tetraarylcyclopentadienones (tetracyclones) or 7,9-diaryl-8H- cyclopentacenaphthylene-8-ones (acecyclones

Polycyclic imide derivatives: Synthesis and effective tuning of lowest unoccupied molecular orbital levels through molecular engineering

Ding, Lin,Ying, Han-Ze,Zhou, Yan,Lei, Ting,Pei, Jian

supporting information; experimental part, p. 5522 - 5525 (2011/02/24)

A series of fluoranthene-fused imide derivatives were facilely developed through a Diels-Alder reaction followed by decarbonylation. The investigation of their photophysical and electrochemical properties demonstrated that their LUMO levels were effective

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