14426-15-4

Basic information

• Product Name: 4-methyl-N-(3-methylbutyl)benzenamine
• Synonyms: 4-methyl-N-(3-methylbutyl)benzenamine
• CAS NO: 14426-15-4
• Molecular Weight: 177.29
• Mol File: 14426-15-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-methyl-N-(3-methylbutyl)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-(3-methylbutyl)benzenamine(14426-15-4)
• EPA Substance Registry System: 4-methyl-N-(3-methylbutyl)benzenamine(14426-15-4)

Safety Data

• Hazardous Substances Data: 14426-15-4(Hazardous Substances Data)

Upstream product

• 123-51-3 i-Amyl alcohol 
• 99-99-0 1-methyl-4-nitrobenzene 
• 100-17-4 para-methoxynitrobenzene 
• 645-41-0 triisoamylamine 
• 106-49-0 p-toluidine 

Relevant articles and documents

Reductive N-alkylation of nitro compounds to N -Alkyl and N, N -dialkyl amines with glycerol as the hydrogen source

As the sustainable and promising hydrogen source, here, glycerol was directly used as the hydrogen source for the reductive amination of alcohol using nitrobenzene as the starting material. The amination of alcohols, especially aliphatic alcohols with different structures, was realized, and mono- or disubstituted amines were synthesized with excellent yields. The reaction mechanism was also explored.

Synthesis of quinolines via ruthenium-catalysed amine exchange reaction between anilines and trialkylamines

Anilines react with an array of trialkylamines in the presence of a catalytic amount of RuCl3*nH2O and bis(diphenylphosphino)methane together with SnCl2*2H2O and hex-1-ene as hydrogen acceptor in dioxane at 180 deg C to afford the corresponding 2,3-disubstituted quinolines in moderate to good yields.