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4-Methyl-N-((E)-pent-2-enyl)-N-prop-2-ynyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

454431-84-6

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454431-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 454431-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,4,3 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 454431-84:
(8*4)+(7*5)+(6*4)+(5*4)+(4*3)+(3*1)+(2*8)+(1*4)=146
146 % 10 = 6
So 454431-84-6 is a valid CAS Registry Number.

454431-84-6Downstream Products

454431-84-6Relevant academic research and scientific papers

Features and applications of [Rh(CO)2Cl]2-catalyzed alkylations of unsymmetrical allylic substrates

Ashfeld, Brandon L.,Miller, Kenneth A.,Smith, Anna J.,Tran, Kristy,Martin, Stephen F.

, p. 9018 - 9031 (2008/03/13)

(Chemical Equation Presented) A novel regio- and stereoselective [Rh(CO)2Cl]2-catalyzed allylic alkylation of unsymmetrical allylic carbonates was discovered. The regioselectivity of the reaction favors product ratios in which substitution occurs at the carbon bearing the leaving group. When an enantiomerically enriched carbonate (≥99% ee) was examined, the Rh(I)-catalyzed allylic alkylation proceeded stereoselectively to provide the alkylation product with retention of absolute stereochemistry (98% ee). To establish the scope of the [Rh(CO)2Cl]2-catalyzed allylic alkylation, a variety of carbon and heteroatom nucleophiles were examined and the results described. As an application of the Rh(I)-catalyzed allylic alkylation, a series of novel domino reactions have been developed that couple the unique regio- and stereoselective [Rh(CO)2Cl]2- catalyzed alkylation of allylic trifluoroacetates with an intramolecular Pauson-Khand annulation, a cycloisomerization, or a [5+2] cycloaddition. A unique aspect of the method described is the use of a single catalyst to effect sequential transformations in which the catalytic activity is moderated simply by controlling the reaction temperature. Implementation of such processes provides a rapid and efficient entry to a variety of bicyclic carbon skeletons from simple precursors.

Diastereoselective cascade synthesis of azabicyclo[3.1.0]hexanes from acyclic precursors

Boehmer, Jutta,Grigg, Ronald,Marchbank, John D.

, p. 768 - 769 (2007/10/03)

The diastereoselective synthesis of azabicyclo[3.1.0]hexanes bearing different substituents on all positions of the cyclopropane ring has been achieved in moderate to good yields.

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