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N-methyl-N-(2,4-dinitrophenyl)glycine methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119548-69-5

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119548-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119548-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,4 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119548-69:
(8*1)+(7*1)+(6*9)+(5*5)+(4*4)+(3*8)+(2*6)+(1*9)=155
155 % 10 = 5
So 119548-69-5 is a valid CAS Registry Number.

119548-69-5Relevant articles and documents

o-Nitroaniline derivatives - 13. Reactions of N-(o-nitroaryl)sarcosine esters with bases

Collins,McFarlane,Mackie,Smith

, p. 7887 - 7898 (2007/10/02)

The title reactions give 1-hydroxy-4-methylquinoxaline-2,3-diones (4) together with a variety of mono- and bi-cyclic byproducts. All of these may result from a common intermediate, viz. a 1-hydroxy-4-methyl-3,4-dihydro-1H-2,1,4-benzoxadiazine-3-carboxylat

REACTIONS OF METHYL ESTERS OF N-(2,4-DINITROPHENYL)GLYCINE AND N-METHYL-N-(2,4-DINITROPHENYL)GLYCINE WITH SODIUM METHOXIDE

Machacek, Vladimir,Sterba, Vojeslav,Kolb, Ivan,Lycka, Antonin

, p. 1044 - 1052 (2007/10/02)

The reaction of methyl ester of N-(2,4-dinitrophenyl)glycine (I) with sodium methoxide produces 5-nitro-2(3H)benzimidazolone (III).The product identity has been proved by its isolation from the reaction mixture under conditions similar to those of kinetic experiments and by independent synthesis.The reaction of methyl ester of N-methyl-N-(2,4-dinitrophenyl)glycine with methoxide proceeds in two steps, the second one being substantially slower.The first step produces N-methyl-2-nitroso-4-nitroaniline (IV), which can be prepared by this reaction in good yield andpurity.N-Methyl-2-nitroso-4-nitroaniline undergoes subsequent reactions in the methoxide solutions.Products of the subsequent reactions have not been identified at the starting ester II concentrations of about 10-4 mol l-1, whereas at higher concentrations of the starting substance the reaction produces 2-amino-2'-methylamino-5,5'-dinitro-ONN-azoxybenzene (V) and 2,2'-bis(methylamino)-5,5'-dinitroazoxybenzene (VI).

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