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(2R,3R)-2-(1-Ethyl-propyl)-3-(4-nitro-phenyl)-oxaziridine is a complex organic compound with the molecular formula C13H16N2O3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of oxaziridines, which are heterocyclic compounds containing an oxirane ring fused to an aziridine ring. The compound features a 4-nitrophenyl group attached to the oxaziridine core, which contributes to its reactivity and potential applications in various chemical transformations. Due to its unique structure and properties, (2R,3R)-2-(1-Ethyl-propyl)-3-(4-nitro-phenyl)-oxaziridine has been studied for its use as a chiral catalyst or ligand in asymmetric synthesis, as well as its potential applications in the pharmaceutical industry.

83326-72-1

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83326-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83326-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,2 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83326-72:
(7*8)+(6*3)+(5*3)+(4*2)+(3*6)+(2*7)+(1*2)=131
131 % 10 = 1
So 83326-72-1 is a valid CAS Registry Number.

83326-72-1Relevant academic research and scientific papers

Stereochemical and Mechanistic Aspects of the Base-catalysed Decomposition of N-Alkyloxaziridines to form NH Ketimines

Boyd, Derek R.,McCombe, Kenneth M.,Sharma, Narain D.

, p. 867 - 872 (2007/10/02)

The synthesis of a new range of oxaziridines (18)-(23), (30)-(35) by peracid oxidation of diaryl ketimines and aryl aldimines is reported.Relatively stable NH ketimine products (24)-(27) have been isolated from base-catalysed decomposition of the oxaziridines (18)-(20), (30)-(35) and a primary kinetic isotope effect (ca. kH/kD 6.0) was observed during decomposition of the oxaziridine trans-(31).The trans-oxaziridines (31)-(35) were found to decompose at a faster rate than the corresponding cis isomers.The relative rates of base-catalysed decomposition of oxaziridine stereoisomers are consistent with a mechanism involving an α-C-H proton abstraction mechanism.

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