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4,4-dimethyl-1-phenyl-6-hepten-1-yn-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

340027-44-3

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340027-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 340027-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,0,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 340027-44:
(8*3)+(7*4)+(6*0)+(5*0)+(4*2)+(3*7)+(2*4)+(1*4)=93
93 % 10 = 3
So 340027-44-3 is a valid CAS Registry Number.

340027-44-3Relevant academic research and scientific papers

The rhodium-catalyzed Pauson-Khand reaction

Kobayashi, Toshitake,Koga, Yuji,Narasaka, Koichi

, p. 73 - 87 (2001)

A rhodium carbonyl complex, [RhCl(CO)2]2, serves as a catalyst of the intra- and inter-molecular Pauson-Khand reaction. By the use of the rhodium catalyst, cyclopentenone derivatives are prepared from various 1,6- and 1,7-enynes unde

A preparation of haloalkylidene cyclopentanones

Cornwall, Nicholas J.,Linehan, Shaun,Weavers, Rex T.

, p. 2919 - 2922 (1997)

A radical-based 5-exo-dig cyclisation, initiated by addition of a trichloromethyl radical to an acyclic acetylenic ketone with an appropriately positioned double bond, has been employed to produce a variety of cyclic haloalkylidene cyclopentanones in mode

Scope of the intramolecular titanocene-catalyzed Pauson-Khand type reaction

Hicks, Frederick A.,Kablaoui, Natasha M.,Buchwald, Stephen L.

, p. 5881 - 5898 (2007/10/03)

A Pauson-Khand type conversion of enynes to bicyclic cyclopentenones employing the commercially available precatalyst titanocene dicarbonyl is described. This methodology shows excellent functional group tolerance for a group 4 metallocene-catalyzed process. The scope and limitations of this cyclization with respect to 1,6-, 1,7- and 1,8-enynes with a variety of terminal alkyne substituents, chiral enynes, and enynes containing substituted olefins are described in detail. A mechanism involving carbonylation of an intermediate titanacyclopentene has been proposed.

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