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2-(1,1,2,2-tetramethyl(ethyleneboronato))-9-(4-tert-butylphenyl)-9-(4-hydroxyphenyl)fluorene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869565-71-9

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869565-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869565-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,5,6 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 869565-71:
(8*8)+(7*6)+(6*9)+(5*5)+(4*6)+(3*5)+(2*7)+(1*1)=239
239 % 10 = 9
So 869565-71-9 is a valid CAS Registry Number.

869565-71-9Downstream Products

869565-71-9Relevant academic research and scientific papers

Synthesis and electrooptical properties of copolymers derived from phenol-functionalized telechelic oligofluorenes

Burnell, Timothy,Cella, James A.,Donahue, Paul,Duggal, Anil,Early, Thomas,Heller, Christian M.,Liu, Jerry,Shiang, Joseph,Simon, David,Slowinska, Katarzyna,Sze, Micah,Williams, Elizabeth

, p. 10667 - 10677 (2008/02/03)

This paper describes the synthesis, characterization, and electrooptical properties of a series of phenol-capped, discrete oligofluorenes with 2, 3, 5, and 7 fluorene units and a statistical oligomer with an average of about 10 fluorene units. Polymers were prepared from the oligomers by various linking reactions through the phenol groups. High molecular weight polycarbonate polymers derived from these oligomers were prepared using BPA-bis-chloroformate (BPABCF) as the linking group. Trends in the optical and electrical properties as a function of oligomer length are reported, Device data for this family of emissive copolymers indicates that charge mobility increases with conjugation length and can be better than that of an analogue homopolymer, A surprising shift in LUMO values due to CFs substitution at the ends of the oligomers was observed.

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