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Bis(2-thienyl) pertelluride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66697-24-3

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66697-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66697-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66697-24:
(7*6)+(6*6)+(5*6)+(4*9)+(3*7)+(2*2)+(1*4)=173
173 % 10 = 3
So 66697-24-3 is a valid CAS Registry Number.

66697-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(thiophen-2-yl)ditelluride

1.2 Other means of identification

Product number -
Other names dithiophen-2-yl ditelluride

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:66697-24-3 SDS

66697-24-3Relevant academic research and scientific papers

Iron-catalyzed formation of C-Se and C-Te bonds through cross coupling of aryl halides with Se(0) and Te(0)/nano-Fe3O4@GO

Kassaee, Mohammadzaman,Motamedi, Elaheh,Movassagh, Barahman,Poursadeghi, Samira

, p. 2337 - 2342 (2013/09/02)

The formation of C-Se and C-Te bonds is of synthetic and biological importance. Graphene oxide based nano-Fe3O4 (nano-Fe 3O4@GO) is used as a reusable catalyst for the efficient synthesis of diselenides and ditellurides, through cross coupling of Se(0) or Te(0) with aryl iodides. The magnetic heterogeneous catalyst could be easily recovered and reused many times without significant loss of catalytic activity. In addition the superiority of nano-Fe3O4@GO over pristine nano-Fe3O4 is established. Georg Thieme Verlag Stuttgart. New York.

2-Thiophenyltellurium derivatives: Alternative synthetic routes and structural characterization

Chauhan, Ashok K.S.,Singh, Poornima,Srivastava, Ramesh C.,Butcher, Ray J.,Duthie, Andrew

experimental part, p. 80 - 86 (2011/10/30)

Grignard reagent prepared from 2-thiophenyl bromide in THF consumes elemental tellurium readily at room temperature and provides a route to obtain bis(2-thiophenyl)ditelluride, Tpn2Te2 (1, Tpn = 2-C 4H3S) in goo

Tellurium in organic synthesis. Preparation of Z-vinylic cuprates from Z-vinylic tellurides and their reaction with enones and epoxides

Tucci, Fabio C.,Chieffi, Andre,Comasseto, Joao V.,Marino, Joseph P.

, p. 4975 - 4989 (2007/10/03)

Z-Vinylic tellurides, obtained with 100% stereoselectivity by the hydrotelluration of acetylenes, are easily transformed into Z-vinylic higher order cyanocuprates by reaction with preformed Me2-Cu(CN)Li2, W-Bu2Cu(CN)Lisub

ORGANOTELLURIUM COMPOUNDS 8. ARYLTELLUROLS AS REDUCING AGENTS

Akiba, Mitsuo,Cava, Michael P.

, p. 1119 - 1128 (2007/10/02)

Phenyltellurol and 2-thienyltellurol, generated in situ, have been found to act as selective reductants towards a number of representative organic substrates.

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