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(2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)methyl 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

881759-96-2

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881759-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881759-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,7,5 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 881759-96:
(8*8)+(7*8)+(6*1)+(5*7)+(4*5)+(3*9)+(2*9)+(1*6)=232
232 % 10 = 2
So 881759-96-2 is a valid CAS Registry Number.

881759-96-2Downstream Products

881759-96-2Relevant academic research and scientific papers

Exomethylene-3,4-ethylenedioxythiophene (emEDOT): A new versatile building block for functionalized electropolymerized poly(3,4-ethylenedioxythiophenes) (PEDOTs)

Sassi, Mauro,Mascheroni, Luca,Ruffo, Riccardo,Salamone, Matteo M.,Pagani, Giorgio A.,Mari, Claudio M.,D'Oorazio, Giuseppe,La Ferla, Barbara,Beverina, Luca

, p. 3502 - 3505 (2013)

A new versatile thiophene derivative exomethylene-3,4- ethylenedioxythiophene (emEDOT) is introduced. The molecule can be straightforwardly prepared in two steps from commercially available derivatives and enables facile further derivatization through both acid catalyzed additions of alcohols and standard thiol-ene click chemistry. The preparation of electrochromic materials and of an electrochemical avidine sensor is shown by the oxidative polymerizations of several functionalized EDOT monomers straightforwardly prepared from emEDOT.

A Phosphonated Poly(ethylenedioxythiophene) Derivative with Low Oxidation Potential for Energy-Efficient Bioelectronic Devices

Hopkins, Jonathan,Fidanovski, Kristina,Travaglini, Lorenzo,Ta, Daniel,Hook, James,Wagner, Pawel,Wagner, Klaudia,Lauto, Antonio,Cazorla, Claudio,Officer, David,Mawad, Damia

, p. 140 - 151 (2022/01/12)

Organic electrochemical transistors (OECTs) for bioelectronic applications require the design of conjugated polymers that are stable in aqueous environments and afford high energy efficiency and good performance in OECTs. Polymers based on poly(ethylenedioxythiophene) (PEDOT) are promising in this area due to their low oxidation potential and reversible redox, but they often require cross-linking to prevent dissolution and yield OECTs operating in the less efficient depletion mode. In this work, a new conjugated polymer PEDOT-Phos is presented, which combines a conjugated poly(ethylenedioxythiophene) (PEDOT) backbone with alkyl-protected phosphonate groups. PEDOT-Phos exhibits a low oxidation onset potential (-0.157 V vs Ag/AgCl) and its nanoporous morphology affords it a high volumetric capacitance (282 ± 62 F cm-3). Without any cross-linking, additives, or post-treatment, PEDOT-Phos can be used in aqueous OECTs with efficient accumulation mode operation, long-term stability when immersed in aqueous media, low threshold voltages (-0.161 ± 0.005 V), good transconductances (9.3 ± 1.8 mS), and ON/OFF current ratios (618 ± 54) comparable to other PEDOT-based materials in OECTs. These results highlight the great promise of PEDOT-Phos as a stand-alone channel material for energy-efficient, bioelectronic devices.

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