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Oxaziridine, 2-(1,1-dimethylethyl)-3,3-diphenyl-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53258-80-3

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53258-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53258-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,5 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53258-80:
(7*5)+(6*3)+(5*2)+(4*5)+(3*8)+(2*8)+(1*0)=123
123 % 10 = 3
So 53258-80-3 is a valid CAS Registry Number.

53258-80-3Upstream product

53258-80-3Relevant academic research and scientific papers

A Study of the Thermal Racemisation of (-)-3,3-Diphenyl-2-(t-butyl)oxaziridine and (-)-1-Chloro-2,2-diphenylaziridine in Several Nematic Solvents using a Microscopic Technique

Spada, Gian Piero,Tampieri, Anna,Gottarelli, Giovanni,Moretti, Irene,Torre, Giovanni

, p. 513 - 516 (2007/10/02)

The thermal racemisation of (-)-3,3-diphenyl-2-(t-butyl)oxaziridine and (-)-1-chloro-2,2-diphenylaziridine in nematic liquid-crystal (LC) solvents has been followed directly on a thermostatic microscopic stage by measuring the variations in time of the diameters of the Grandjean-Cano disclination circles, which are associated with the induced cholesteric structure.With respect to isotropic solvents, the nematic phases exert relevant influences on the process, affecting both the activation enthalpy and entropy.Although the two variations partially compensate, the first-order rate constants are smaller in the nematic solvents.

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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