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(2R,3R)-3-(4-Bromo-phenyl)-2-tert-butyl-oxaziridine is a chiral, synthetic organic compound characterized by its oxaziridine ring structure. It features a 4-bromo-phenyl group attached to the 3-position and a tert-butyl group at the 2-position, both of which are in the R configuration. (2R,3R)-3-(4-Bromo-phenyl)-2-tert-butyl-oxaziridine is known for its reactivity and is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its ability to act as a chiral auxiliary or a reactive intermediate in asymmetric transformations. Its unique structure and properties make it a valuable tool in organic chemistry for the development of enantioselective reactions and the creation of complex molecular architectures.

62058-74-6

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62058-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62058-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,5 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62058-74:
(7*6)+(6*2)+(5*0)+(4*5)+(3*8)+(2*7)+(1*4)=116
116 % 10 = 6
So 62058-74-6 is a valid CAS Registry Number.

62058-74-6Relevant academic research and scientific papers

Weak base-promoted selective rearrangement of oxaziridines to amidesviavisible-light photoredox catalysis

Park, Jin,Park, Sehoon,Jang, Gwang Seok,Kim, Ran Hui,Jung, Jaehoon,Woo, Sang Kook

supporting information, p. 9995 - 9998 (2021/10/06)

The selective rearrangement of oxaziridines to amidesviaa single electron transfer (SET) pathway is unexplored. In this study, we present a weak base-promoted selective rearrangement of oxaziridines to amidesviavisible-light photoredox catalysis. The developed method shows excellent functional group tolerance with a broad substrate scope and good to excellent yields. Furthermore, control experiments and density functional theory (DFT) calculations are performed to gain insight into the reactivity and selectivity.

Atom economical synthesis of: N -alkylbenzamides via the iron(III) sulfate catalyzed rearrangement of 2-alkyl-3-aryloxaziridines in water and in the presence of a surfactant

Kra?em, Jamil,Ollevier, Thierry

supporting information, p. 1263 - 1267 (2017/08/15)

A green and mild synthetic route to N-alkylbenzamides involves eco-friendly one pot synthesis of 2-alkyl-3-aryloxaziridines from N-alkylamines and benzaldehydes followed by iron(iii) sulfate catalyzed rearrangement to the corresponding amides in water as the solvent and in the presence of sodium dodecyl sulfate as the surfactant. This green approach affords N-alkylbenzamides in high overall yields under simple and minimum manipulation.

Imines and Derivatives. Part 24. Nitrone Synthesis by Imine Oxidation using either a Peroxyacid or Dimethyldioxirane

Boyd, Derek R.,Coulter, Peter B.,McGuckin, M. Rosaleen,Sharma, Narain D.,Jennings, W. Brian,Wilson, Valerie E.

, p. 301 - 306 (2007/10/02)

The oxidation of N-alkyl imines by m-chloroperoxybenzoic acid to yield nitrones was facilitated by (i) the presence of C-aryl substituents, (ii) steric inhibition of attack at the imino C-atom, (iii) electron donating para-substituents on the C-aryl substituent, (iv) non-hydroxylic solvents, (v) optimal conjugation between C-aryl substituents and the imino group, and (vi) less bulky N-alkyl groups. The oxidation of N-alkyl imines by dimethyldioxirane (DMD) in dichloromethane-acetone solution yielded nitrones without evidence of oxaziridine formation.The yields of isolated nitrones were higher for C,C-diaryl imines and for imines bearing less bulky N-alkyl substituents.N-H substituted ketimines were found to yield oximes after reaction with dimethyldioxirane.

Synthesis of 2-Alkyl-3-aryloxaziridines

Kloc, Krystian,Kubicz, Elzbieta,Mlochowski, Jacek,Syper, Ludwik

, p. 1084 - 1087 (2007/10/02)

A convenient method for the synthesis of 2-alkyl-3-aryloxaziridines 1 based on the formation of stable azomethines and their oxidation with m-chloroperoxybenzoic acid is reported.The scope and limitation of the method proposed is illustrated with numerous

DYNAMIC STEREOCHEMISTRY OF IMINES AND DERIVATIVES. PART 18. PHOTOSYNTHESIS AND PHOTORACEMIZATION OF OPTICALLY ACTIVE OXAZIRIDINES

Boyd, Derek R.,Campbell, Rose M.,Coulter, Peter B.,Grimshaw, James,Neill, David C.,Jennings, W. Brian

, p. 849 - 856 (2007/10/02)

Optically active oxaziridines have been synthesized with a maximum optical yield of 31percent by photoisomerization (λ > 300 nm) of achiral aldo- and keto-nitrones in the presence of the chiral solvent (+)-(S) or (-)-(R)-2,2,2-trifluoro-1-phenylethanol.Ph

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