6247-00-3

Basic information

• Product Name: N,N-DIALLYLANILINE
• Synonyms: 2-Propen-1-amine, N-phenyl-N-2-propenyl-;Benzenamine, N,N-di-2-propenyl-;Diallyl-phenyl-amine;N,N-Dipropen-3-ylaniline;N,N-DIALLYLANILINE;Ai3-09527;Aniline, N,N-diallyl- (8ci);Benzenamine, N,N-di-2-propenyl- (9ci)
• CAS NO: 6247-00-3
• Molecular Formula: C₁₂H₁₅N
• Molecular Weight: 173.25
• Product Categories: monomer
• Mol File: 6247-00-3.mol
• Article Data: 83

Chemical Properties

• Boiling Point: 250.4 °C at 760 mmHg
• Flash Point: 101.3 °C
• Appearance: /
• Density: 0.943 g/cm³
• Vapor Pressure: 0.0217mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: N,N-DIALLYLANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DIALLYLANILINE(6247-00-3)
• EPA Substance Registry System: N,N-DIALLYLANILINE(6247-00-3)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 6247-00-3(Hazardous Substances Data)

Usage

General Description

N,N-Diallylaniline is a chemical compound with the formula C12H15N. It is a clear to slightly yellow liquid that is insoluble in water but soluble in organic solvents. This chemical is commonly used as a monomer in the production of various polymers and copolymers. It is also utilized as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, N,N-Diallylaniline can be used as a crosslinking agent and as a co-monomer in the production of resins and adhesives. It is important to handle this chemical with care as it is considered to be a hazardous substance with potential harmful effects if not properly managed.

InChI:InChI=1/C12H15N/c1-3-10-13(11-4-2)12-8-6-5-7-9-12/h3-9H,1-2,10-11H2

Upstream product

• 106-95-6 allyl bromide 
• 62-53-3 aniline 
• 107-05-1 3-chloroprop-1-ene 
• 557-40-4 Allyl ether 
• 107-18-6 allyl alcohol 
• 109-72-8 n-butyllithium 
• 98-95-3 nitrobenzene 
• 589-09-3 N-allyl-N-phenylamine 
• 622-37-7 Phenyl azide 
• 100191-80-8 N-allyl-N-(prop-2-ynyl)benzeneamine 
• 556-56-9 allyl iodid 
• 591-87-7 Allyl acetate 
• 201230-82-2 carbon monoxide 
• 124-02-7 diallylamine 

Downstream Products

• 75176-71-5 4-diallylamino-benzaldehyde 
• 589-09-3 N-allyl-N-phenylamine 
• 187737-37-7 propene 
• 74-85-1 ethene 
• 62-53-3 aniline 
• 16078-94-7 N,N-di-2-propenylbenzeneamine 
• 5278-43-3 3-methyl-2-phenyl-quinoline 
• 758640-21-0 N-Benzylaniline 
• 30438-95-0 N,N-diallyl-4-bromobenzenamine 
• 36127-28-3 N,2-diallylaniline 
• 175032-68-5 N,N,N',N'-tetraallylbiphenyl-4,4'-diamine 
• 101130-93-2 N,N-diallyl-4-nitrobenzenamine 
• 635-90-5 1-phenylpyrrole 
• 103204-12-2 1-phenyl-2,5-dihydro-1H-pyrrole 

Relevant articles and documents

Intramolecular cooperativity in frustrated Lewis pairs

The doubly Lewis-acid functionalised aniline PhN[(CH2)3B(C6F5)2]2 features two competing boron functions in fast exchange for binding to the central Lewis base. It shows catalytic activity typical for FLPs in H/D-scrambling and catalytic hydrogenation experiments. By contrast, the singly acid-functionalised PhMeN(CH2)3B(C6F5)2 reveals a dramatically smaller catalytic activity in analogous experiments.

Highly efficient Ru(ii)-alkylidene based Hoveyda-Grubbs catalysts for ring-closing metathesis reactions

Three novel phosphine-free Ru-alkylidenes (7a-7c) have been synthesized and utilized as efficient catalysts for ring closing metathesis (RCM) reaction. Spectroscopic data, i.e. NMR and HRMS, along with single crystal X-ray diffraction analysis, were used

Heterobimetallic Eu(iii)/Pt(ii) single-chain nanoparticles: a path to enlighten catalytic reactions

We introduce the formation and characterization of heterometallic single-chain nanoparticles entailing both catalytic and luminescent properties. A terpolymer containing two divergent ligand moieties, phosphines and phosphine oxides, is synthesized and intramolecularly folded into nanoparticlesviaa selective metal complexation of Pt(ii) and Eu(iii). The formation of heterometallic Eu(iii)/Pt(ii) nanoparticles is evidenced by size exclusion chromatography, multinuclear NMR (1H,31P{1H},19F,195Pt) as well as diffusion-ordered NMR and IR spectroscopy. Critically, we demonstrate the activity of the SCNPs as a homogeneous and luminescent catalytic system in the amination reaction of allyl alcohol.