138200-69-8

Basic information

• Product Name: Benzenamine, N-methyl-4-nitro-N-propyl-
• CAS NO: 138200-69-8
• Molecular Formula: C10H14N2O2
• Molecular Weight: 194.233
• Mol File: 138200-69-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-methyl-4-nitro-N-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-methyl-4-nitro-N-propyl-(138200-69-8)
• EPA Substance Registry System: Benzenamine, N-methyl-4-nitro-N-propyl-(138200-69-8)

Safety Data

• Hazardous Substances Data: 138200-69-8(Hazardous Substances Data)

Upstream product

• 13395-54-5 N-methyl-N-n-propylaniline 
• 6032-29-7 (+/-)-2-pentanol 
• 100-01-6 4-nitro-aniline 
• 50-00-0 formaldehyd 
• 123-38-6 propionaldehyde 

Relevant articles and documents

An efficient conversion of nitroaromatics and aromatic amines to tertiary amines in one-pot way

Reductive alkylation and reductive methylation of aromatic primary amines with carbonyls and 37% formaldehyde using decaborane in one-pot way gave the corresponding tertiary amines in high yields. The reaction condition was extended for the reduction of n

N-Dealkylation-N-nitrosation of Tertiary Aromatic Amines by n-Butyl Nitrite

N,N-Dialkyl aromatic amines with a variety of ring substituents are N-dealkylated and N-nitrosated efficiently by n-butyl nitrite/ammonium chloride/water at reflux temperature.Ring nitrosation was never observed, but minor amounts of m- and p-nitro amines and/or nitrosamines were formed in some cases.Ring nitration is rather a reaction of the initial substrate than a process occurring on formed nitrosamines.The leaving propensities of the initial N-substituents to yield nitrosamines were in the order benzyl >> methyl >> alkyl.Key Words: Nitrosamines; N-Dealkylation; N-Nitrosation; C-Nitration; Alkyl nitrite.