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1,4-Benzenediacetonitrile, 2,5-bis(dodecyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

737581-58-7

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737581-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 737581-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,7,5,8 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 737581-58:
(8*7)+(7*3)+(6*7)+(5*5)+(4*8)+(3*1)+(2*5)+(1*8)=197
197 % 10 = 7
So 737581-58-7 is a valid CAS Registry Number.

737581-58-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(cyanomethyl)-2,5-didodecoxyphenyl]acetonitrile

1.2 Other means of identification

Product number -
Other names 1,4-bis(cyanomethyl)-2,5-bis(dodecyloxy)benzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:737581-58-7 SDS

737581-58-7Downstream Products

737581-58-7Relevant academic research and scientific papers

Spectral broadening in MEH-PFV:PCBM-based photovoltaic devices via blending with a narrow band gap cyanovinylene-dioxythiophene polymer

Thompson, Barry C.,Kim, Young-Gi,Reynolds, John R.

, p. 5359 - 5362 (2005)

A novel narrow band gap polymer and illustrations of the design principles for developing an ideal donor polymer with proper electronic band structure requirements in a comprehensive manner were described. The cyanovinylene linkage may serve as a Michael

Copolymers for iodide detection and methods thereof

-

Page/Page column 6; 26, (2020/02/03)

Copolymers having thiophene based and vinylene based moieties. Methods of producing the copolymers, and methods of utilizing the copolymers as chromogenic sensors for selective detection of iodide anion are also provided.

Soluble narrow band gap and blue propylenedioxythiophene-cyanovinylene polymers as multifunctional materials for photovoltaic and electrochromic applications

Thompson, Barry C.,Kim, Young-Gi,McCarley, Tracy D.,Reynolds, John R.

, p. 12714 - 12725 (2008/02/05)

A family of soluble narrow band gap donor-acceptor conjugated polymers based on dioxythiophenes and cyanovinylenes is reported. The polymers were synthesized using Knoevenagel polycondensation or Yamamoto coupling polymerizations to yield polymers with molecular weights on the order of 10 000-20 000 g/mol, which possess solubility in common organic solvents. Thin film optical measurements revealed narrow band gaps of 1.5-1.8 eV, which gives the polymers a strong overlap of the solar spectrum. The energetic positions of the band edges were determined by cyclic voltammetry and differential pulse voltammetry and demonstrate that the polymers are both air stable and show a strong propensity for photoinduced charge transfer to fullerene acceptors. Such measurements also suggest that the polymers can be both p- and n-type doped, which is supported by spectroelectrochemical results. These polymers have been investigated as electron donors in photovoltaic devices in combination with PCBM ([6,6]-phenyl C61-butyric acid methyl ester) as an electron acceptor based on the near ideal band structures designed into the polymers. Efficiencies as high as 0.2% (AM1.5) with short circuit current densities as high as 1.2-1.3 mA/cm2 have been observed in polymer/PCBM (1:4 by weight) devices and external quantum efficiencies of more than 10% have been observed at wavelengths longer than 600 nm. The electrochromic properties of the narrow band gap polymers are also of interest as the polymers show three accessible color states changing from an absorptive blue or purple in the neutral state to a transmissive sky-blue or gray in the oxidized and reduced forms. The wide electrochemical range of electrochromic activity coupled with the strong observed changes in transmissivity between oxidation states makes these materials potentially interesting for application to electrochromic displays.

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