59472-05-8

Basic information

• Product Name: N-(2-methylbutyl)aniline
• Synonyms: N-(2-methylbutyl)aniline
• CAS NO: 59472-05-8
• Molecular Weight: 163.263
• Mol File: 59472-05-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(2-methylbutyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-methylbutyl)aniline(59472-05-8)
• EPA Substance Registry System: N-(2-methylbutyl)aniline(59472-05-8)

Safety Data

• Hazardous Substances Data: 59472-05-8(Hazardous Substances Data)

Upstream product

• 137-32-6 (+/-)-2-methyl-1-butanol 
• 62-53-3 aniline 
• 96-17-3 2-Methylbutyraldehyde 
• 98-95-3 nitrobenzene 
• 6668-42-4 2-methyl-1-phenylbutan-1-one oxime 
• 54394-78-4 2-methylbutanoic acid anilide 
• 10422-35-2 1-bromo-2-methyl-butane 
• 589-09-3 N-allyl-N-phenylamine 
• 557-18-6 diethylmagnesium 

Relevant articles and documents

Solvent-free one-pot reduction of imines generated in situ from aldehydes and aniline by tributyltin hydride on silica gel

Imines generated in situ from aldehydes and aniline can be reduced using tributyltin hydride on silica gel under solvent-free conditions to provide the corresponding amines in good yields.

Method for synthesizing N-alkyl arylamine

The invention discloses a method for synthesizing N-alkyl arylamine. The method comprises the steps of adding amine, alcohol, a metal iridium catalyst, alkali to a reaction vessel for reflux reaction,cooling to room temperature after reaction, spin-drying a solvent and then conducting separation on columns to obtain a target compound. According to the method for synthesizing the N-alkyl arylamine, a series of N-benzylaniline derivatives are prepared by using transition metal iridium as the catalyst, weak base is used, by-product is water, and a product has relatively good yield, and has certain applicable value.

Chiral organometallic compounds

A chiral, organometallic compound which, at a molecular level, has no C2 symmetry and comprises a carbon to carbon bond joining a chiral carbon atom to a carbon atom of a cyclopentadiene ring that is non-symmetrically substituted. Examples of such compounds include compounds of formula (I): STR1 wherein X1 and X2 are, independently, groups which are removable during a chemical reaction; M is titanium, zirconium or hafnium; and R1-8,11 are as specified in the description.