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1,3,2-Dioxaborolane, 2-(5-bromo-4-hexyl-2-thienyl)-4,4,5,5-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

906006-56-2

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906006-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906006-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,0,0 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 906006-56:
(8*9)+(7*0)+(6*6)+(5*0)+(4*0)+(3*6)+(2*5)+(1*6)=142
142 % 10 = 2
So 906006-56-2 is a valid CAS Registry Number.

906006-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-bromo-4-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-(5-bromo-4-hexylthiophen-2-yl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane

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:906006-56-2 SDS

906006-56-2Downstream Products

906006-56-2Relevant academic research and scientific papers

Suzuki route to regioregular polyalkylthiophenes using Ir-catalysed borylation to make the monomer, and Pd complexes of bulky phosphanes as coupling catalysts for polymerisation

Liversedge, Iain A.,Higgins, Simon J.,Giles, Mark,Heeney, Martin,McCulloch, Iain

, p. 5143 - 5146 (2006)

We have applied palladium complexes of bulky, electron-rich phosphane ligands as catalysts for the Suzuki synthesis of highly head-to-tail regioregular polyalkylthiophenes from 2-(5-bromo-4-n-alkyl-thiophen-2-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane. The monomer can be prepared in high yield by Ir-catalysed borylation of 2-bromo-3-hexylthiophene, without the need for organolithium reagents or strong bases.

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