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181218-41-7

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181218-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181218-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,1 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 181218-41:
(8*1)+(7*8)+(6*1)+(5*2)+(4*1)+(3*8)+(2*4)+(1*1)=117
117 % 10 = 7
So 181218-41-7 is a valid CAS Registry Number.

181218-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-bis(chloromethyl)-3,4-diphenylthiophene

1.2 Other means of identification

Product number -
Other names -

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:181218-41-7 SDS

181218-41-7Relevant articles and documents

Synthesis of 3,4-diphenyl-substituted poly(thienylene vinylene), low-band-gap polymers via the dithiocarbamate route

Henckens,Colladet,Fourier,Cleij,Lutsen,Gelan,Vanderzande

, p. 19 - 26 (2007/10/03)

It has been demonstrated that the dithiocarbamate precursor route is a suitable pathway towards poly(thienylene vinylene) (PTV)-type low-band-gap polymers. Two particular dithiocarbamate precursor polymers and the corresponding conjugated polymers, poly(3,4-diphenyl-2,5-thienylene vinylene) and poly(3,4-bis(4-butylphenyl)-2,5-thienylene vinylene), have been studied. The introduction of butyl side chains in the latter leads to excellent solubility in common organic solvents. Both polymers have been prepared in a straightforward manner and in good yield. The thermal conversion of the precursor polymers into the conjugated structure was studied with in situ FT-IR and UV-vis spectroscopy. Also, with the latter technique, the band gap was determined and the thermochromic effect was studied and compared with the unsubstituted PTV. The HOMO and LUMO levels of the polymers were determined from UV-vis and electrochemical measurements.

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