6247-00-3 Usage
Description
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.
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
6247-00-3Relevant articles and documents
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.
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
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.
