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(2R,3R)-3-(3-Nitro-phenyl)-2-(toluene-4-sulfonyl)-oxaziridine is a complex organic compound with the molecular formula C16H14N2O5S. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of oxaziridines, which are three-membered heterocyclic compounds containing an oxygen and a nitrogen atom. The compound features a 3-nitrophenyl group attached to the oxaziridine ring, and a toluene-4-sulfonyl group as a substituent. This specific arrangement of functional groups endows the molecule with unique chemical properties and reactivity, making it potentially useful in various chemical transformations and synthetic applications, particularly in the field of asymmetric synthesis.

67995-01-1

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67995-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67995-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,9 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67995-01:
(7*6)+(6*7)+(5*9)+(4*9)+(3*5)+(2*0)+(1*1)=181
181 % 10 = 1
So 67995-01-1 is a valid CAS Registry Number.

67995-01-1Relevant academic research and scientific papers

Chemistry of Oxaziridines. 1. Synthesis and Structure of 2-Arenesulfonyl-3-aryloxaziridines. A New Class of Oxaziridines

Davis, Franklin A.,Lamendola, Joseph,Nadir, Upender,Kluger, Edward W.,Sedergran, Thomas C.,et al.

, p. 2000 - 2005 (2007/10/02)

A new class of oxaziridine derivatives, 2-arenesulfonyl-3-aryloxaziridines (2), is prepared by m-CPBA oxidation of sulfonimines (RSO2N=CHAr).These compounds are the first stable examples of this ring system to have a substituent other than carbon attached to nitrogen and are characterized by a highly electrophilic oxaziridine oxygen atom.These oxaziridines have the E configuration as determined by X-ray crystallography.The presence of the powerful electron-attracting sulfonyl group attached to nitrogen apparently has little effect on the structure of the oxaziridine three-membered ring.Of more significance are the observations that the nitrogen lone pair in 2 is opposite to one of the sulfonyl oxygens and that the long S-N bond length implies little if any conjugative interaction between sulfur and nitrogen.Attempts to prepare oxaziridines via oxidation of sulfonimines, 5, derived from acetophenone gave imidoyl ether 14, a novel Baeyer-Villiger oxidation product of a C-N double bond.

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