103170-53-2 Usage
Uses
Used in Organic Synthesis:
N-Methyl-6-nitro-5-quinolinaMine is used as a synthetic intermediate for the preparation of various organic compounds. Its unique chemical structure allows it to be a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-Methyl-6-nitro-5-quinolinaMine is used as a key intermediate in the synthesis of various drug molecules. Its presence in the molecular structure can impart specific biological activities, making it a valuable component in the development of new therapeutic agents.
Used in Agrochemical Industry:
N-Methyl-6-nitro-5-quinolinaMine is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness in controlling pests and diseases, thereby contributing to increased crop yields and food security.
Check Digit Verification of cas no
The CAS Registry Mumber 103170-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,7 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103170-53:
(8*1)+(7*0)+(6*3)+(5*1)+(4*7)+(3*0)+(2*5)+(1*3)=72
72 % 10 = 2
So 103170-53-2 is a valid CAS Registry Number.
103170-53-2Relevant academic research and scientific papers
Oxidative Methylamination of Nitroquinolines
Wozniak, Marian,Grzegozek, Maria
, p. 823 - 830 (2007/10/02)
3-, 5-, 6-, 7- and 8-nitroquinoline as well as 5,7- and 6,8-dinitroquinoline are methylaminated with a liquid methylamine solution of potassium permanganate (LMA/PP) to the corresponding mono- and bis(methylamino)-substituted compounds. 2-Nitroquinoline is aminated with LMA/PP to 2-(methylamino)quinoline.The intermediate methylamino ?-adducts of 3-nitro- and 5,7- and 6,8-dinitroquinoline are detected by 1H-NMR spectroscopy.Quantum chemical calculations for the mononitroquinolines suggest that the experimentally observed regioselectivity of the methylamination is controlled by an interaction of frontal molecular orbitals (FMO) of the reagents. Key Words: Methylaminations / ?-Adducts, methylamino / Calculations, FMO / Quinolines / Aminations
