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ethyl 3,5-diphenylthiophene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23806-17-9

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23806-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23806-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,0 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23806-17:
(7*2)+(6*3)+(5*8)+(4*0)+(3*6)+(2*1)+(1*7)=99
99 % 10 = 9
So 23806-17-9 is a valid CAS Registry Number.

23806-17-9Downstream Products

23806-17-9Relevant academic research and scientific papers

Rhodium Thiavinyl Carbenes from 1,2,3-Thiadiazoles Enable Modular Synthesis of Multisubstituted Thiophenes

Kurandina, Daria,Gevorgyan, Vladimir

, p. 1804 - 1807 (2016)

The rhodium-catalyzed transannulation reaction between 1,2,3-thiadiazoles and alkynes, proceeding via intermediacy of the previously unknown Rh thiavinyl carbene, toward a highly efficient and regioselective synthesis of up to fully substituted thiophenes is described.

Utilizing an Encapsulated Solution of Reagents to Achieve the Four-Component Synthesis of (Benzo)Thiophene Derivatives

Shen, Chaoren,Spannenberg, Anke,Auer, Matthias,Wu, Xiao-Feng

supporting information, p. 941 - 946 (2017/03/27)

Reagent capsules can help to resolve the compatibility problem of reagents in multicomponent processes. Herein we demonstrate a facile method for encapsulating smelly liquid chemicals and its application in a modular palladium-catalyzed carbonylative synthesis of multi-substituted thiophenes from terminal alkynes and aryl iodides as well as a palladium-catalyzed carbonylative synthesis of benzothiophene derivatives from aryl iodides and arylboronic acids. Here, the capsule plays a pivotal role in solving the issues on reaction condition incompatibilities and selectivity of multicomponent reactions as well as avoiding deactivation of the catalyst by releasing the reagents when the reaction temperature is raised. It greatly facilitates the development of highly-efficient multicomponent reactions and demonstrates a modular pathway to obtain functionalized molecules. (Figure presented.).

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