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(+/-)-1-(3-butynyl)-2-methylenecyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

348135-65-9

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348135-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 348135-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,8,1,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 348135-65:
(8*3)+(7*4)+(6*8)+(5*1)+(4*3)+(3*5)+(2*6)+(1*5)=149
149 % 10 = 9
So 348135-65-9 is a valid CAS Registry Number.

348135-65-9Downstream Products

348135-65-9Relevant academic research and scientific papers

Investigation of the synthesis of angular tricyclic compounds by intramolecular Pauson-Khand reaction of exo- and endo-cyclic enynes

Ishizaki,Iwahara,Niimi,Satoh,Hoshino

, p. 2729 - 2738 (2007/10/03)

Intramolecular Pauson-Khand reaction of various alkynyl exo-alkylidene-cyclohexanes and -pentane gives angular type 6-5-5 and 5-5-5 tricyclic compounds in good to high yield. The present reaction also offers convenient construction of two contiguous quaternary centers, which could not be synthesized from alkynyl endo-cycloolefins. Scope and limitation of the present reaction of various exo- and endo-cyclic enynes are also described.

Titanocene catalysed 5-exo cyclisations of unsaturated epoxides- reagent control in radical chemistry

Gansaeuer,Pierobon,Bluhm

, p. 2500 - 2520 (2007/10/03)

A synthetic route to carbocyclic and heterocyclic [3.3.0], [4.3.0] and [5.3.0] systems containing pyrrolidine and tetrahydrofuran units and various other tetrahydrofuran derivatives is presented. The products are of relevance for natural product synthesis and for the synthesis of biologically active compounds. The titanocene catalysed reactions utilises readily available unsaturated epoxides as substrates. A model explaining the diastereoselectivity of cyclisation is presented that should allow for rational design of more selective catalysts.

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