27125-60-6

Basic information

• Product Name: N-(3-methylbut-2-en-1-yl)aniline
• CAS NO: 27125-60-6
• Molecular Formula: C₁₁H₁₅N
• Molecular Weight: 161.2435
• Mol File: 27125-60-6.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 259.5°C at 760 mmHg
• Flash Point: 111.5°C
• Density: 0.957g/cm³
• Vapor Pressure: 0.0129mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: N-(3-methylbut-2-en-1-yl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-methylbut-2-en-1-yl)aniline(27125-60-6)
• EPA Substance Registry System: N-(3-methylbut-2-en-1-yl)aniline(27125-60-6)

Safety Data

• Hazardous Substances Data: 27125-60-6(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 78-79-5 isoprene 
• 598-25-4 Dimethylallene 
• 107-86-8 3,3-dimethyl acrylaldehyde 
• 98-95-3 nitrobenzene 
• 3422-01-3 tert-butyl phenylcarbamate 
• 870-63-3 prenyl bromide 
• 3009-97-0 N-phenylglycinonitrile 
• 115-18-4 2-methyl-3-buten-2-ol 
• 556-82-1 3-methyl-2-buten-1-ol 
• 861373-31-1 N-(3-methyl-but-2-enyl)-formanilide 
• 199472-25-8 3-(o-bromophenyl)-2-[N-(3-methylbutenyl)anilino]propanenitrile 
• 83036-58-2 prenyl diisopropyl phosphate 
• 503-60-6 3,3-dimethyl-allyl chloride 

Downstream Products

• 132704-05-3 (3-Methyl-but-2-enyl)-phenyl-carbamic acid ethyl ester 
• 1402238-83-8 N-(3-methylbut-2-en-1-yl)-N-phenylbenzimidamide 
• 1402238-86-1 1,2-diphenyl-4-(prop-1-en-2-yl)-4,5-dihydro-1H-imidazole 
• 20972-43-4 trans-azoxybenzene 
• 132704-06-4 2-(1-Chloro-1-methyl-ethyl)-4-(toluene-4-sulfonyl)-3,4-dihydro-2H-benzo[1,4]thiazine 
• 132704-03-1 4-methyl-N-(3-methylbut-2-enyl)-N-phenylbenzenesulfonamide 
• 2051-84-5 N-isopentylaniline 
• 83703-55-3 (3-Methyl-but-2-enyl)-((E)-1-methyl-but-2-enyl)-phenyl-amine 
• 16466-48-1 N-isopentyl-N-phenylbenzamide 

Relevant articles and documents

Catalytic Selective Oxidative Coupling of Secondary N-Alkylanilines: An Approach to Azoxyarene

Azoxyarenes are among important scaffolds in organic molecules. Direct oxidative coupling of primary anilines provides a concise fashion to construct them. However, whether these scaffolds can be prepared from secondary N-alkylanilines is not well explored. Here, we present a catalytic selective oxidative coupling of secondary N-alkylaniline to afford azoxyarene with tungsten catalyst under mild conditions. In addition, azoxy can be viewed as a bioisostere of alkene and amide. Several "azoxyarene analogues" of the corresponding bioactive alkenes and amides showed comparable promising anticancer activities.

Flow synthesis of secondary amines over Ag/Al2O3 catalyst by one-pot reductive amination of aldehydes with nitroarenes

An alumina-supported silver catalyst was investigated in the one-pot reductive amination of aldehydes with nitroarenes in a continuous flow reactor using molecular hydrogen as a reducing agent. A series of secondary amines containing alkyl, OH, OCH3, Cl, Br and CC groups was synthesized in good to excellent yields. The yield of the secondary amine depends on the rate of formation of an intermediate imine. It was shown that the accumulation of carbonaceous deposits on the catalyst is the main reason of catalyst deactivation. The spent catalyst can be easily regenerated and reused without losing catalytic activity.

Synthetic method of allylamine

The invention provides a synthetic method of allylamine compounds with substituted allyl alcohol and aromatic amines as raw materials through induction of a titanium metal intermediate. The invention relates to a secondary amine substituted by an allyl gr