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3,6-di(2,6-dimethylphenyl)-9H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1246891-46-2

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1246891-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1246891-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,8,9 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1246891-46:
(9*1)+(8*2)+(7*4)+(6*6)+(5*8)+(4*9)+(3*1)+(2*4)+(1*6)=182
182 % 10 = 2
So 1246891-46-2 is a valid CAS Registry Number.

1246891-46-2Downstream Products

1246891-46-2Relevant academic research and scientific papers

Dendritic bipolar main body material taking triazine as central core, and preparation method and application of dendritic bipolar main body material in organic electroluminescent device

-

, (2020/08/26)

The invention provides a compound with a structure represented by a formula (I) and a preparation method and application thereof. The compound with the structure represented by the formula (I) is a dendritic bipolar main body material taking triazine as a central core, the structure is different from a D-pi-A type structure of a traditional dendritic bipolar main body; the central core triazine isused as an electron acceptor (A), peripheral branches are used as electron donors (D), and a D-A type dendritic bipolar main body formed by direct connection of the donors and the acceptors maintainsa high triplet state energy level (2.8-3.3 eV), so that the application of the bipolar main body to a blue light OLED device is facilitated; it is found through experiments that the maximum current efficiency of a blue phosphorus photoluminescence device prepared with the compound as a main body material can reach 46.7 cd/A, the maximum power efficiency can reach 50.11 m/W, the maximum brightnesscan reach 32000 cd/m, and the turn-on voltage is 2.4 V.

Enantioselective synthesis of butadien-2-ylcarbinols via (silylmethyl)allenic alcohols from chromium-catalyzed additions to aldehydes utilizing chiral carbazole ligands

Durán-Galván, María,Worlikar, Shilpa A.,Connell, Brian T.

scheme or table, p. 7707 - 7719 (2010/10/21)

The synthesis of chiral, nonracemic butadienylcarbinols by employing intermediate (trimethylsilyl)methylallenic alcohols is described. Allenic alcohols are obtained by treatment of aldehydes with (4-bromobut-2-ynyl) trimethylsilane in the presence of a ca

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