Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 693-67-4, is researched, Molecular C11H23Br, about Reactivity Ratios of MMA and N,N-Dimethyl-N-{2-[(2-methylprop-2-enoyl)oxy]ethyl}undecane-1-aminium Bromide in Thermal and UV Initiation Copolymerization, the main research direction is reactivity MMA dimethylmethylpropenoyloxyethylundecaneaminium bromide copolymerization.Synthetic Route of C11H23Br.
Reactivity ratios for the copolymerization of Me methacrylate (MMA) and a quaternary ammonium compound (QAC) N,N-dimethyl-N-{2-[(2-methylprop-2-enoyl)oxy]ethyl}undecane-1-aminium bromide (dMEMUABr) were measured for the first time by using a thermal initiator azobisisobutyronitrile (AIBN) in deuterated DMSO (DMSO-d6) and deuterated chloroform (CDCl3) and a photo initiator 2-hydroxy-2-methylpropiophenone (HMP) under UV irradiation in CDCl3, resp. The consumption profiles for monomer in the thermal initiation copolymerization were monitored by in-situ 1H NMR while the data were analyzed by the Meyo-Lewis, Kelen-Tudos, and Meyer-Lowry methods, showing that the reactivity ratio of dMEMUABr is lower than that of MMA in DMSO-d6 but much higher in CDCl3. The significantly different reactivity ratios of dMEMUABr in DMSO-d6 from that in CDCl3 are attributed to micelle formation. These findings enable addnl. flexibility in the design and development of antimicrobial poly(MMA-co-dMEMUABr) coatings with desired copolymer chain sequence.
There is still a lot of research devoted to this compound(SMILES：CCCCCCCCCCCBr)Synthetic Route of C11H23Br, and with the development of science, more effects of this compound(693-67-4) can be discovered.
Reference:
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem