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7042-08-2

Cis-1-(4-nitrobenzoyl)-2,3-diphenylaziridine is a complex organic chemical compound with the molecular formula C20H16N2O3. It is characterized by its aziridine ring, which is a three-membered nitrogen-containing ring, and its 4-nitrobenzoyl group, which is a benzoic acid derivative with a nitro group at the para position. The compound also features two phenyl groups attached to the 2 and 3 positions of the aziridine ring, which contribute to its stability and reactivity. This molecule is of interest in organic chemistry due to its potential applications in the synthesis of pharmaceuticals and other specialty chemicals, as well as its unique structural properties that can influence its chemical behavior.

7042-08-2

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7042-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7042-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7042-08:
(6*7)+(5*0)+(4*4)+(3*2)+(2*0)+(1*8)=72
72 % 10 = 2
So 7042-08-2 is a valid CAS Registry Number.

7042-08-2Relevant articles and documents

RuV-Acylimido Intermediate in [RuIV(Por)Cl2]-Catalyzed C–N Bond Formation: Spectroscopic Characterization, Reactivity, and Catalytic Reactions

Che, Chi-Ming,Hong, Dan-Yan,Huang, Jie-Sheng,Law, Siu-Man,Liu, Yungen,Lo, Vanessa Kar-Yan,Toy, Patrick H.,Wu, Liangliang

supporting information, p. 18619 - 18629 (2021/06/09)

Metal-catalyzed C?N bond formation reactions via acylnitrene transfer have recently attracted much attention, but direct detection of the proposed acylnitrenoid/acylimido M(NCOR) (R=aryl or alkyl) species in these reactions poses a formidable challenge. H

Asymmetric ring opening reactions of symmetrical N-acylaziridines with thiols catalyzed by chiral dialkyl tartrate-diethylzinc complexes

Hayashi, Masahiko,Ono, Kazuyuki,Hoshimi, Haruhisa,Oguni, Nobuki

, p. 7817 - 7832 (2007/10/03)

The asymmetric ring opening reaction of 1,2-(N-acylimino)cyclohexanes (N- acylaziridines) with some thiols proceeded in the presence of chiral zinc complexes prepared from diethylzinc and dialkyl L-(+)-tartrate to afford trans 2-(N-acylamino)-1-arylthiocyclohexane in up to 93% cc. The enantioselectivity is highly influenced by the molar ratio of the reactants and the nature of chiral dialkyl tartrate. The chemical structure of dialkyl L-(+)-tartrate-zinc complex is discussed on their 1H NMR spectra and molecular weight.

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