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Benzene, 1-methyl-4-[(phenylethynyl)telluro]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56950-08-4

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56950-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56950-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,5 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56950-08:
(7*5)+(6*6)+(5*9)+(4*5)+(3*0)+(2*0)+(1*8)=144
144 % 10 = 4
So 56950-08-4 is a valid CAS Registry Number.

56950-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4-(2-phenylethynyltellanyl)benzene

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:56950-08-4 SDS

56950-08-4Downstream Products

56950-08-4Relevant academic research and scientific papers

Synthesis of alkynyltellurides mediated by K3PO4 and DMSO

Do Sacramento, Manoela,Menezes, Larissa,Goldani, Bruna,Perin, Gelson,Silva, Marcio S.,Barcellos, Thiago,Alves, Diego

supporting information, p. 11091 - 11098 (2019/07/31)

In the present work, a simple method for the synthesis of alkynyltellurides is described by the reactions of terminal alkynes with diorganyl ditellurides in the presence of a catalytic amount of K3PO4. In both substrates, it was possible to vary the aryl and alkyl groups, obtaining the products of interest in short reaction times and in yields ranging from 30 to 93%. This methodology, different from those already reported in the literature, has the advantage of using a catalytic amount of a weak base and no use of metallic catalysts.

Magnetite (Fe3O4) nanoparticles: An efficient and recoverable catalyst for the synthesis of alkynyl chalcogenides (selenides and tellurides) from terminal acetylenes and diorganyl dichalcogenides

Godoi, Marcelo,Liz, Daiane G.,Ricardo, Eduardo W.,Rocha, Manuela S.T.,Azeredo, Juliano B.,Braga, Antonio L.

, p. 3349 - 3354 (2014/05/06)

We present herein a new and efficient methodology for the synthesis of alkynyl chalcogenides from terminal acetylenes and diorganyl dichalcogenides, catalyzed by Fe3O4 nanoparticles. This new approach provided the desired products in good to excellent yields. Moreover, the catalyst was easily recoverable using an external magnet and reused for further experiments without loss of catalytic activity.

A General and highly efficient protocol for the synthesis of chalcogenoacetylenes by copper(I)-terpyridine catalyst

Movassagh, Barahman,Yousefi, Ali,Momeni, Badri Zaman,Heydari, Sepideh

, p. 1385 - 1390 (2014/06/23)

A highly efficient copper-catalyzed Csp-X (X = S, Se, Te) bond-forming reaction of terminal alkynes and diorganyl dichalcogenides has been developed. This transformation was realized through the use of copper(I) iodide as a catalyst, 4′-(4-meth

Cesium hydroxide-catalyzed reaction of terminal alkynes with diarylditellurides to synthesize alkynyl tellurides

Zou, Kang Bing,Qiu, Ren Hua,Fang, Da Wei,Liu, Xin You,Xu, Xin Hua

, p. 2237 - 2242 (2008/09/21)

In the presence of a catalytic amount of cesium hydroxide under an air atmosphere, the reaction of diarylditellurides (1.0 mmol) with terminal alkynes (2.2 mmol) at room temperature exclusively give alkynyl tellurides in good yields. Copyright Taylor & Fr

Hypervalent iodine in synthesis XXVI: A convenient synthesis of acetylenic tellurides

Zhang, Jun-Lian,Chen, Zhen-Chu

, p. 3881 - 3885 (2007/10/03)

Acetylenic tellurides have been prepared by the reaction of sodium arenetellurolates with alkynylphenyliodonium tosylates in DMF.

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