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(Z)-7-bromo-4'-(methylsulfonyl)-5-heptenophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

217454-47-2

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217454-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217454-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,4,5 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 217454-47:
(8*2)+(7*1)+(6*7)+(5*4)+(4*5)+(3*4)+(2*4)+(1*7)=132
132 % 10 = 2
So 217454-47-2 is a valid CAS Registry Number.

217454-47-2Downstream Products

217454-47-2Relevant academic research and scientific papers

Intramolecular cyclization of tethered phenyl ketones. Complementary stereochemical results arising from the indium-promoted ring closure of allyl bromides and the fluoride ion-induced desilylation of allylsilanes

Paquette, Leo A.,Mendez-Andino, Jose L.

, p. 9061 - 9068 (2007/10/03)

The intramolecular indium-promoted cyclization of 4'-substituted (Z)- and (E)-7-bromo-5-heptenophenones has been examined in aqueous tetrahydrofuran. In every instance, ring closure occurred to deliver the syn- 2-vinylcyclopentanol exclusively. The corresponding allylsilanes have been prepared as well, and the course of their fluoride ion-induced cyclization was also studied. In these systems, a kinetic bias for formation of the anti- 2-vinylcyclopentanol is observed, although not with the same exclusivity. Accordingly, complementarity in product diastereoselectivity can be realized in purposeful fashion. The data acquired in this investigation suggest that the indium-catalyzed reactions involve intramolecularly coordinated transition states where development of a cis 5/6-bicyclic framework is most energetically feasible. In contrast, the silanes appear to utilize open- chain antiperiplanar transition states. While the latter are not particularly sensitive to double-bond geometry, they are responsive to steric compression involving the aryl group.

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