101906-08-5

Basic information

• Product Name: N-butyl-4-phenoxyaniline
• Synonyms: N-butyl-4-phenoxyaniline
• CAS NO: 101906-08-5
• Molecular Weight: 241.333
• Mol File: 101906-08-5.mol

Chemical Properties

• CAS DataBase Reference: N-butyl-4-phenoxyaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-butyl-4-phenoxyaniline(101906-08-5)
• EPA Substance Registry System: N-butyl-4-phenoxyaniline(101906-08-5)

Safety Data

• Hazardous Substances Data: 101906-08-5(Hazardous Substances Data)

Upstream product

• 102-82-9 tributyl-amine 
• 139-59-3 4-phenoxyanilin 
• 101480-27-7 N-(4-Phenoxy-phenyl)-butyramide 

Downstream Products

• 123-72-8 butyraldehyde 
• 139-59-3 4-phenoxyanilin 

Relevant articles and documents

Conversion of Primary Amines to Symmetrical Secondary and Tertiary Amines using a Co-Rh Heterobimetallic Nanocatalyst

Symmetrical tertiary amines have been efficiently realized from amine and secondary amines via deaminated homocoupling with heterogeneous bimetallic Co2Rh2/C as catalyst (molar ratio Co:Rh=2:2). Unsymmetric secondary anilines were produced from the reaction of anilines with symmetric tertiary amines. The Co2Rh2/C catalyst exhibited very high catalytic activity towards a wide range of amines and could be conveniently recycled ten times without considerable leaching. (Figure presented.).

Bis(salicylaldehyde)ethylenedi-iminecobalt(II)-catalysed Oxidation of Aromatic Amins with Oxygen

N-n-Butylanilines undergo N-dealkylation to give a primary amine and butyrylaldehyde by oxidation with oxygen in the presence of bis(salicylaldehyde)ethylenedi-iminecobalt(II) (CoIIsalen) as a catalyst.High conversions are obtained with high catalyst concentrations and low / ratios (r).Inspection of the effect of catalyst and substrate concentrations on initial reaction rates (Vin) shows poor sensitivity to the electronic effect of the nuclear substituent.Some anilines give azo derivatives at a lower rate in the same conditions.