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1-(2-chlorophenyl)methyl-2-(phenoxymethyl)aziridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

883199-55-1

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883199-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883199-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,1,9 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 883199-55:
(8*8)+(7*8)+(6*3)+(5*1)+(4*9)+(3*9)+(2*5)+(1*5)=221
221 % 10 = 1
So 883199-55-1 is a valid CAS Registry Number.

883199-55-1Relevant academic research and scientific papers

Cobalt carbonyl-catalyzed carbonylation of functionalized aziridines to versatile β-lactam building blocks

Piens, Nicola,Van Hecke, Kristof,Vogt, Dieter,D'Hooghe, Matthias

supporting information, p. 4816 - 4821 (2017/07/10)

The Co2(CO)8-catalyzed carbonylation of different classes of non-activated aziridines with diverse substitution patterns was investigated. Special attention was devoted to selectivity issues and reaction optimization. This study resu

Systematic study of halide-induced ring opening of 2-substituted aziridinium salts and theoretical rationalization of the reaction pathways

D'Hooghe, Matthias,Catak, Saron,Stankovic, Sonja,Waroquier, Michel,Kim, Yongeun,Ha, Hyun-Joon,Van Speybroeck, Veronique,De Kimpe, Norbert

experimental part, p. 4920 - 4931 (2010/10/03)

The ring-opening reactions of 2-alkyl-substituted l,1-bis(arylmethyl)- and 1-methyl-1-(l-phenylethyl)aziridinium salts with fluoride, chloride, bromide and iodide in acetonitrile have been, evaluated for the first: time in a systematic way. The reactions

A new approach towards 2-amino-1-aryloxy-3-methoxypropanes from 1-arylmethyl-2-(bromomethyl)aziridines

D'Hooghe, Matthias,Waterinckx, Alex,Vanlangendonck, Tim,De Kimpe, Norbert

, p. 2295 - 2303 (2007/10/03)

1-Arylmethyl-2-(bromomethyl)azirdines were converted into the corresponding 2-(aryloxymethyl)aziridines upon treatment with the appropriate potassium phenoxides in DMF/acetone in excellent yields, followed by regioselective ring opening towards N,N-di(ary

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