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 
• 4873-09-0 allyl tosylate 
• 589-09-3 N-allyl-N-phenylamine 
• 6728-21-8 allyl mesylate 
• 622-37-7 Phenyl azide 
• 119803-83-7 allyl pheny telluroxide 
• 557-40-4 Allyl ether 
• 116808-70-9 cyclopropyldiphenylsulfonium triflate 
• 124-02-7 diallylamine 
• 98-80-6 phenylboronic acid 
• 107-18-6 allyl alcohol 
• 100-46-9 benzylamine 

Downstream Products

• 16078-94-7 N,N-di-2-propenylbenzeneamine 
• 103204-12-2 1-phenyl-2,5-dihydro-1H-pyrrole 
• 589-09-3 N-allyl-N-phenylamine 
• 6625-74-7 N-pivaloylaniline 
• 1598463-88-7 N-(2-(4-(diallylamino)phenyl)-2-phenylvinyl)-4-methylbenzenesulfonamide 
• 1598463-89-8 N-(2-(4-(diallylamino)phenyl)-2-phenylvinyl)-4-methylbenzenesulfonamide 
• 1316312-93-2 allyl-(2-allylphenyl)phenylamine 
• 1316312-68-1 1-phenyl-2,5-dihydro-1H-benzo[b]azepine 
• 74-85-1 ethene 
• 158924-97-1 Co(N,N-diallylaniline)(PMe₃)2 
• 158924-90-4 Ni(N,N-diallylaniline)P(CH₃)3 
• 158924-97-1 {(1,2,3,6,7-η5)-4-phenyl-4-aza-2,6-heptadienyl}bis(trimethylphosphane)cobalt(I) 
• 149206-56-4 N-phenyl-2-pyrroline 
• 5278-43-3 3-methyl-2-phenyl-quinoline 

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

RED FLUORESCENT PROBE FOR USE IN DETECTION OF PEPTIDASE ACTIVITY

[Problem] A problem addressed by the present invention is to provide a novel fluorescent probe having excellent tissue permeability that is capable of detecting the peptidase activity expressed at a high level in cancer cells and the like as a response of long-wavelength red fluorescence. [Solution] A compound represented by formula (I) or a salt thereof: [In the formula, A represents a ring structure selected from the group consisting of a thiophene ring, a cyclopentene ring, a cyclopentadiene ring, and a furan ring; X represents a C0-C3 alkylene group;Y represents O, S, C(═O)O, or NH,Z represents O, C(Ra) (Rb), Si(Ra) (Rb), Ge(Ra) (Rb), Sn(Ra) (Rb), Se, P(Rc), or P(Rc) (═O) (where Ra and Rb each independently represent a hydrogen atom or an alkyl group, and Rc represents a hydrogen atom, an alkyl group, or an aryl group);R1 and R2 each independently represent from one to three of the same or different substituents selected from the group consisting of a hydrogen atom, a hydroxyl group, a halogen atom, and an alkyl group, a sulfo group, a carboxyl group, an ester group, an amide group, and an azide group each of which may be substituted;R3 represents an acyl residue derived from an amino acid (where the acyl residue is a residue obtained by removing an OH group from a carboxyl group of the amino acid);R4 and R5 each independently represent a hydrogen atom or an alkyl group (where when R4 or R5 is an alkyl group, the R4 or R5, together with R2, may form a ring structure comprising a nitrogen atom to which R4 and R5 are bonded).]