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2-Thiopheneacetic acid, 5-phenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62689-80-9

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62689-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62689-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,8 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62689-80:
(7*6)+(6*2)+(5*6)+(4*8)+(3*9)+(2*8)+(1*0)=159
159 % 10 = 9
So 62689-80-9 is a valid CAS Registry Number.

62689-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(5-phenylthiophen-2-yl)acetate

1.2 Other means of identification

Product number -
Other names 2-Thiopheneacetic acid,5-phenyl-,methyl ester

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:62689-80-9 SDS

62689-80-9Upstream product

62689-80-9Downstream Products

62689-80-9Relevant academic research and scientific papers

Direct C-H Arylation of Heteroarenes with Copper Impregnated on Magnetite as a Reusable Catalyst: Evidence for CuO Nanoparticle Catalysis in Solution

Vásquez-Céspedes, Suhelen,Chepiga, Kathryn M.,M?ller, Nadja,Sch?fer, Andreas H.,Glorius, Frank

, p. 5954 - 5961 (2016)

A reusable copper-based catalyst system was employed for the direct arylation of electron-rich heteroarenes. Under mild and operationally simple reaction conditions good yields and selectivities were obtained using diaryliodonium salts as coupling partners. A combination of experimental methods including kinetic studies, filtration tests, and a series of analytical tools (TXRF, ICP-MS, SEM, XPS, TEM, EFTEM) provide evidence for catalytically active soluble nanoparticles formed from an amorphous heterogeneous precursor. Mechanistic studies hint at a redox-neutral process which promotes counterion dissociation from the diaryliodonium salt by a copper(II) oxide species.

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