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1-(5-chloro-2-methylthien-3-yl)-2-[5-(dibutoxyboryl)-2-methylthien-3-yl]cyclopentene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

509083-62-9

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509083-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 509083-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,9,0,8 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 509083-62:
(8*5)+(7*0)+(6*9)+(5*0)+(4*8)+(3*3)+(2*6)+(1*2)=149
149 % 10 = 9
So 509083-62-9 is a valid CAS Registry Number.

509083-62-9Upstream product

509083-62-9Relevant academic research and scientific papers

Design, syntheses and photochromic properties of dithienylcyclopentene optical molecular switches

Yu, Chuanming,Hu, Bingcheng,Liu, Cheng,Li, Jiting

, (2016/12/22)

A kind of basal diarylethene through an easy synthetic procedure was synthesized and characterized, and a Suzuki coupling reaction was frequently operated to obtain the diarylethenes derivatives with some vivid functional groups like bromo, amido and pyridine. Two methods for derivatives of these switches contain porphyrins were described. All of their spectroscopic and photochromic properties were studied and intercompared. It is indicated that the difference in electron densities of the π-conjugated system of the closed forms has effects upon the absorption maxima in visible region of UV–Vis spectra. Dithienylcyclopentenes linked to porphyrins could emit luminescence substantially that display potentials to be used in the applications of nondestructive readout upon binary data storage and smart materials.

Syntheses of dithienylcyclopentene optical molecular switches

Lucas, Linda N.,De Jong, Jaap J. D.,Van Esch, Jan H.,Kellogg, Richard M.,Feringa, Ben L.

, p. 155 - 166 (2007/10/03)

Properly functionalized dithienylethenes show promise for light-induced switching processes. To prevent cis/trans isomerization from competing with conrotatory 6π-electron ring closure, the ethene segment is usually incorporated in a (perfluorinated) cyclopentene. In the present article syntheses of perhydrocyclopentene 1 and perfluorocyclopentene 2 are described, which are amenable for large-scale conversions. Both compounds have chloro substituents at the 5-position of the thiophene rings to allow further functionalization. The conversion of the chloro substituents of 1 to formyl, carboxylate, boronyl, and hydrogen groups by halogen/lithium exchange at room temperature is described, and examples are given of further elaboration of 1 and 2 by attachment, both in a symmetrical as well as unsymmetrical fashion, of additional functionality by condensation, Friedel-Crafts or Suzuki reactions. The newly prepared thienylperhydrocyclopentene derivatives show reversible photochromism if the substituents at the 5-postions allow for conjugation with the thiophene π-system. Wiley-VCH Verlag GmbH & Co KGaA, 69451 Weinheim, Germany, 2003.

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