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(+)-(E)-{2-[(S)-N-methyl-S-phenylsulfonimidoyl]ethenyl}benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147600-83-7

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147600-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147600-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,0 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147600-83:
(8*1)+(7*4)+(6*7)+(5*6)+(4*0)+(3*0)+(2*8)+(1*3)=127
127 % 10 = 7
So 147600-83-7 is a valid CAS Registry Number.

147600-83-7Relevant academic research and scientific papers

Synthesis of phosphanyl sulfoximines through phospha-michael reaction of alkenyl sulfoximines and their evaluation as chiral bidentate 1, 5-N, P ligands for palladium in asymmetric allylic alkylation

Lemasson, Fabien,Gais, Hans-Joachim,Runsink, Jan,Raabe, Gerhard

experimental part, p. 2157 - 2175 (2010/06/16)

The intermolecular phospha-Michael reaction of cyclic and acyclic alkenyl sulfoximines proceeds readily and yields the corresponding phosphanyl sulfoximines in good yield. The asymmetric induction provided, by sulfoximine group in C-P bond formation is ap

S-Ethenylsulfoximine Derivatives. Reagents for Ethylenation of Protic Nucleophiles

Johnson, Carl R.,Lockard, James P.,Kennedy, Eugene R.

, p. 264 - 271 (2007/10/02)

The preparation of S-vinyl and S-(2-substituted)ethenyl derivatives of sulfoximines is described.Vinyl-, (2-phenylethenyl)-, (2,2-diphenylethenyl)-, (2-methyl-1-propenyl)-, (dimethylamino)phenyloxosulfonium fluoroborates were found to undergo an addition-elimination reaction sequence with protic nitrogen and carbon nucleophiles, resulting in ethylenation of the nucleophile and N,N-dimethylbenzenesulfinamide.Primary amines gave aziridines, enamines gave cyclopropyl derivatives of iminium salts or pyrrolidinium salts, anions of active methylene compounds gave dihydrofurans and/or cyclopropanes, and anions of nitroalkanes gave cyclic nitronic esters and/or nitrocyclopropanes.In several cases vinyl salts were generated in situ from β-methoxyoxosulfonium salts.Treatment of (-)-(S)-dimethylamino)phenyl(trans-2-phenylethenyl)oxosulfonium fluoroborate with methyl cyanoacetate in methanol containing sodium methoxide gave, in 81percent yield, (+)-(1S,2R)-methyl 1-cyano-2-phenylcyclopropanecarboxylate of 25.5percent optical purity.The same salt upon treatment with methyl nitroacetate gave, in 95percent yield, methyl 4-phenyl-3-isoxazolinecarboxylate 2-oxide with 33percent enantiomeric excess.Cyclopropanes were formed upon treatment of S-methyl-S-(trans-2-phenylethenyl)-N-(p-tolylsulfonyl)sulfoximine with anions of active methylene compounds.

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