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204191-77-5

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204191-77-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204191-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,1,9 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 204191-77:
(8*2)+(7*0)+(6*4)+(5*1)+(4*9)+(3*1)+(2*7)+(1*7)=105
105 % 10 = 5
So 204191-77-5 is a valid CAS Registry Number.

204191-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-5-(2,3,4,5,6-pentafluorophenyl)thiophene

1.2 Other means of identification

Product number -
Other names 2-perfluorophenyl-5-bromothiophene

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:204191-77-5 SDS

204191-77-5Downstream Products

204191-77-5Relevant articles and documents

n-Type Thiophene Semiconductors

-

Page/Page column 8; 15, (2009/01/20)

The new fluorocarbon-functionalized and/or heterocycle-modified polythiophenes, in particular, α,ω-diperfluorohexylsexithiophene DFH-6T can be straightforwardly prepared in high yield and purity. Introduction of such modifications to a thiophene core affords enhanced thermal stability and volatility, and increased electron affinity versus the unmodified compositions of the prior art. Evaporated films behave as n-type semiconductors, and can be used to fabricate thin film transistors with FET mobilities ?0.01 cm2/Vs—some of the highest reported to date for n-type organic semiconductors.

Perfluorophenylation of aromatic and heteroaromatic compounds with pentafluorobenzenesulfonyl chloride catalyzed by a ruthenium (ii) phosphine complex

Kamigata, Nobumasa,Yoshikawa, Manabu,Shimizu, Toshio

, p. 91 - 95 (2007/10/03)

The reactions of pentafluorobenzenesulfonyl chloride with benzene and thiophene derivatives in the presence of a ruthenium(II) catalyst proceeded at 240°C, with extrusion of sulfur dioxide and hydrogen chloride, to give the corresponding perfluorophenylated compounds.

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