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5-bromo-3,3',3,3'''-tetrahexyl-2,2':5':5',5:2,2'''-quaterthiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170702-21-3

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170702-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170702-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,7,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 170702-21:
(8*1)+(7*7)+(6*0)+(5*7)+(4*0)+(3*2)+(2*2)+(1*1)=103
103 % 10 = 3
So 170702-21-3 is a valid CAS Registry Number.

170702-21-3Upstream product

170702-21-3Relevant academic research and scientific papers

A successful chemical strategy to induce oligothiophene self-assembly into fibers with tunable shape and function

Di Maria, Francesca,Olivelli, Pasquale,Gazzano, Massimo,Zanelli, Alberto,Biasiucci, Mariano,Gigli, Giuseppe,Gentili, Denis,D'Angelo, Pasquale,Cavallini, Massimiliano,Barbarella, Giovanna

, p. 8654 - 8661 (2011/07/29)

Functional supramolecular architectures for bottom-up organic nano- and microtechnology are a high priority research topic. We discovered a new recognition algorithm, resulting from the combination of thioalkyl substituents and head-to-head regiochemistry of substitution, to induce the spontaneous self-assembly of sulfur overrich octathiophenes into supramolecular crystalline fibers combining high charge mobility and intense fluorescence. The fibers were grown on various types of surfaces either as superhelices or straight rods depending on molecular structure. Helical fibers directly grown on a field effect transistor displayed efficient charge mobility and intrinsic 'memory effect'. Despite the fact that the oligomers did not have chirality centers, one type of hand-helicity was always predominant in helical fibers, due to the interplay of molecular atropisomerism and supramolecular helicity induced by terminal substituents. Finally, we found that the new sulfur overrich oligothiophenes can easily be prepared in high yields through ultrasound and microwave assistance in green conditions.

Synthesis and Properties of α,ω-Disubstituted Oligo(3-hexylthiophene)s and Oligothienoquinonoids in Head-to-head Orientation

Higuchi, Hiroyuki,Nakayama, Taketoshi,Koyama, Haruki,Ojima, Juro,Wada, Tatsuo,Sasabe, Hiroyuki

, p. 2363 - 2378 (2007/10/03)

The two types of Highly-ordered oligo(3-hexylthiophene)s in head-to-head orientation, a series od α,ω-disubstituted oligothiophenes and a series of bis(dicyanomethylene)oligothienoquinonoids, were synthesized.The properties of these compounds are discussed on the basis of the electronic spectra and cyclic voltammetry.

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