Welcome to LookChem.com Sign In|Join Free
  • or
N,N-Diallylaniline, with the chemical formula C12H15N, is a clear to slightly yellow liquid that is insoluble in water but soluble in organic solvents. It is a versatile chemical compound commonly used as a monomer in the production of various polymers and copolymers, as well as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, it serves as a crosslinking agent and a co-monomer in the production of resins and adhesives. Due to its hazardous nature, it is crucial to handle N,N-Diallylaniline with care to avoid potential harmful effects.

6247-00-3

Post Buying Request

6247-00-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6247-00-3 Usage

Uses

Used in Polymer and Copolymer Production:
N,N-Diallylaniline is used as a monomer for the production of various polymers and copolymers, contributing to the formation of materials with specific properties and applications.
Used in Pharmaceutical and Agrochemical Synthesis:
N,N-Diallylaniline is utilized as a building block in the synthesis of pharmaceuticals and agrochemicals, playing a crucial role in the development of new drugs and agricultural chemicals.
Used in Resin and Adhesive Production:
N,N-Diallylaniline is used as a crosslinking agent and a co-monomer in the production of resins and adhesives, enhancing the bonding and structural properties of these materials.
Used in Chemical Industry:
In the chemical industry, N,N-Diallylaniline is used as a monomer for the synthesis of various compounds and materials, contributing to the development of new products and technologies.
Used in Research and Development:
N,N-Diallylaniline is employed in research and development settings to explore its potential applications and properties, further expanding its use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6247-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6247-00:
(6*6)+(5*2)+(4*4)+(3*7)+(2*0)+(1*0)=83
83 % 10 = 3
So 6247-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15N/c1-3-10-13(11-4-2)12-8-6-5-7-9-12/h3-9H,1-2,10-11H2

6247-00-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-DIALLYLANILINE

1.2 Other means of identification

Product number -
Other names N,N-di-2-propenylaniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6247-00-3 SDS

6247-00-3Relevant academic research and scientific papers

Intramolecular cooperativity in frustrated Lewis pairs

K?rte, Leif A.,Blomeyer, Sebastian,Heidemeyer, Shari,Mix, Andreas,Neumann, Beate,Mitzel, Norbert W.

, p. 9949 - 9952 (2016)

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.

Copper-Catalyzed Allylation of Amines with Cyclopropyldiphenylsulfonium Trifluoromethanesulfonate

Ma, Yu,Tian, Ze-Yu,Zhang, Cheng-Pan,Zheng, Shuang-Yang

, (2022/03/15)

Cyclopropyldiphenylsulfonium salt, a famous ylide precursor previously extensively employed in the preparation of cyclic compounds, has been successfully utilized as an efficient allylation reagent in this work. The copper-catalyzed reactions of cyclopropyldiphenylsulfonium trifluoromethanesulfonate with amines in the presence of an appropriate ligand provided the N-allylated products in good yields. Aliphatic/ aromatic amines and primary/secondary amines were all converted under mild reaction conditions. This protocol was also applicable to N-functionalization of drug molecules, supplying the corresponding N-allylated compounds in satisfactory yields. The reaction, which showed good functional group tolerance with a wide range of substrates and excellent chemoselectivity, offers an interesting method for the synthesis of N-allyl amines.

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

Al-Awadi, Nouria A.,Al-Enezi, Mariam Y.,Ibrahim, Yehia A.,John, Elizabeth

, p. 37866 - 37876 (2021/12/09)

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

A base-free Chan–Lam reaction catalyzed by an easily assembled Cu(II)-carboxylate metal-organic framework

Ma, Ruixuan,Qin, Jianhua,Shi, Lei,Zhang, Xinhai

, p. 795 - 799 (2021/07/06)

A new copper(II) metal-organic framework is constructed as a sustainable copper heterogeneous catalyst. Cu-DPTCA, with high catalytic activity, can effectively promote the Chan–Lam coupling reaction of arylboronic acids and amines without adding any base or additive.

RED FLUORESCENT PROBE FOR USE IN DETECTION OF PEPTIDASE ACTIVITY

-

Paragraph 0086; 0088, (2020/03/28)

[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).]

Multicolor Activatable Raman Probes for Simultaneous Detection of Plural Enzyme Activities

Fujioka, Hiroyoshi,Kamiya, Mako,Kojima, Ryosuke,Ozeki, Yasuyuki,Shou, Jingwen,Urano, Yasuteru

supporting information, p. 20701 - 20707 (2020/12/23)

Raman probes based on alkyne or nitrile tags hold promise for highly multiplexed imaging. However, sensing of enzyme activities with Raman probes is difficult because few mechanisms are available to modulate the vibrational response. Here we present a gen

Spontaneously Blinking Fluorophores Based on Nucleophilic Addition/Dissociation of Intracellular Glutathione for Live-Cell Super-resolution Imaging

Morozumi, Akihiko,Kamiya, Mako,Uno, Shin-Nosuke,Umezawa, Keitaro,Kojima, Ryosuke,Yoshihara, Toshitada,Tobita, Seiji,Urano, Yasuteru

supporting information, p. 9625 - 9633 (2020/07/25)

Single-molecule localization microscopy (SMLM) allows the reconstruction of super-resolution images but generally requires prior intense laser irradiation and in some cases additives to induce blinking of conventional fluorophores. We previously introduced a spontaneously blinking rhodamine fluorophore based on an intramolecular spirocyclization reaction for live-cell SMLM under physiological conditions. Here, we report a novel principle of spontaneous blinking in living cells, which utilizes reversible ground-state nucleophilic attack of intracellular glutathione (GSH) upon a xanthene fluorophore. Structural optimization afforded two pyronine fluorophores with different colors, both of which exhibit equilibrium (between the fluorescent dissociated form and the nonfluorescent GSH adduct form) and blinking kinetics that enable SMLM of microtubules or mitochondria in living cells. Furthermore, by using spontaneously blinking fluorophores working in the near-infrared (NIR) and green ranges, we succeeded in dual-color live-cell SMLM without the need for optimization of the imaging medium.

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

Barner-Kowollik, Christopher,Kn?fel, Nicolai D.,Kulendran, Bragavie,Roesky, Peter W.,Rothfuss, Hannah,Tzvetkova, Pavleta

, p. 10331 - 10336 (2020/10/18)

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.

Dehydrative Allylation of Amine with Allyl Alcohol by Titanium Oxide Supported Molybdenum Oxide Catalyst

Kon, Yoshihiro,Nakashima, Takuya,Fujitani, Tadahiro,Murayama, Toru,Ueda, Wataru

supporting information, p. 287 - 292 (2019/02/12)

The dehydrative allylation from allyl alcohol with amines to generate various allyl amines by MoO 3 /TiO 2 solid catalyst is described. The catalyst can be reused at least three times without a decrease of activity.

SUPER-RESOLUTION FLUORESCENT IMAGING PROBE

-

Paragraph 0133; 0134; 0135; 0136, (2018/03/25)

[Problem] To provide a novel fluorescent probe for super-resolution imaging that uses fluorescent light emission characteristics that originate from an intermolecular nucleophilic addition-dissociation equilibrium reaction, and to provide a super-resoluti

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6247-00-3