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3,3'-(2,2'-(ethyne-1,2-diyl)bis(2,1-phenylene))dihex-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268367-93-6

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1268367-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268367-93-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,3,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1268367-93:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*6)+(3*7)+(2*9)+(1*3)=196
196 % 10 = 6
So 1268367-93-6 is a valid CAS Registry Number.

1268367-93-6Downstream Products

1268367-93-6Relevant academic research and scientific papers

Synthesis of biaryl compounds using tandem ruthenium-catalyzed ring-closing metathesis

Yoshida, Kazuhiro,Shida, Hiroaki,Takahashi, Hidetoshi,Yanagisawa, Akira

supporting information; experimental part, p. 344 - 349 (2011/02/27)

Tandem ring-closing enyne metathesis (RCEM)/ring-closing olefin metathesis (RCM) of tetraenynes with Grubbs second-generation catalyst, followed by elimination, was found to be a new and efficient synthetic approach to biaryl compounds. A preliminary asymmetric version of this approach, which used homochiral Ru-alkylidene catalysts, is also presented. A ringing endorsement: Tandem ring-closing enyne metathesis (RCEM)/ring-closing olefin metathesis (RCM) of tetraenynes with the Grubbs second-generation catalyst followed by elimination, was found to be a new and efficient synthetic approach to biaryl compounds (see scheme). A preliminary asymmetric version of this approach is also presented.

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