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2-methyl-5,5-di-p-tolylpenta-2,3,4-trienal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

912663-55-9

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912663-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 912663-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,6,6 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 912663-55:
(8*9)+(7*1)+(6*2)+(5*6)+(4*6)+(3*3)+(2*5)+(1*5)=169
169 % 10 = 9
So 912663-55-9 is a valid CAS Registry Number.

912663-55-9Relevant academic research and scientific papers

Domino Heck-C-H activation reaction of unsymmetrically substituted [3]cumulene

Furuta, Takumi,Asakawa, Tomohiro,Iinuma, Mie,Fujii, Satoshi,Tanaka, Kiyoshi,Kan, Toshiyuki

, p. 3648 - 3650 (2006)

The Heck reaction of an unsymmetrically substituted [3]cumulene has been investigated. Although a carbonyl conjugated alkene is present, the arylpalladium species selectively inserts into the C3-4 double bond, and a subsequent C-H activation reaction with a neighboring phenyl group gives the indene derivatives with a tetrasubstituted olefin moiety. The Royal Society of Chemistry 2006.

Reaction behavior of cumulene: Diels-Alder, Friedel-Crafts, and Pb-catalyzed domino reactions

Asakawa, Tomohiro,Iinuma, Mie,Wakasugi, Yuko,Kuno, Mayumi,Furuta, Takumi,Fujii, Satoshi,Tanaka, Kiyoshi,Kan, Toshiyuki

experimental part, p. 1125 - 1147 (2010/10/02)

Diels-Alder, Friedel-Crafts, and domino reactions mediated by Pd-catalyst of [3]cumulene 1 were investigated. Although the Diels-Alder reaction with cyclopentadiene occurred selectively on the C2, C3 double bond to give tetrasubstituted allenyl products, the Friedel-Crafts type addition of electron-rich heteroaromatics and subsequent protonation cleanly occurred on the C3, C4 double bond to afford tetrasubstituted conjugated dienes. In the Heck reaction with aryl iodide, the arylpalladium species was selectively inserted into the C3, C4 double bond and a subsequent C-H activation reaction with a neighboring phenyl group gave indene derivatives with a tetrasubstituted olefin moiety. Furthermore, Pd-catalyzed domino cyclization-allylation reaction of in situ generated [3]cumulene alkoxide afforded tetrasubstituted furan.

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