Little discovery in the laboratory: a new route for 111-24-0

Although many compounds look similar to this compound(111-24-0)Related Products of 111-24-0, numerous studies have shown that this compound(SMILES:BrCCCCCBr), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Synthesis and characterization of cationic quaternary ammonium geminis (16-s-16) and their role in ninhydrin-[Cu(II)-His]+ reaction, published in 2021, which mentions a compound: 111-24-0, Name is 1,5-Dibromopentane, Molecular C5H10Br2, Related Products of 111-24-0.

Cationic quaternary ammonium gemini surfactants were synthesized by mixing N,N-dimethylcetylamine and α,ω-dibromoalkane. The synthesized products were characterized by C, H, N elemental and 1H NMR analyses. The critical micelle concentration (CMC) of these surfactants with and without additives was calculated by means of the conductivity technique. The role of the synthesized quaternary ammonium geminis in the reaction was investigated by a UV-vis spectroscopy. The rate constant (kψ) was determined at different gemini concentrations and plotted graphically as kψ vs. [16-s-16]. Addnl., the influence of other reaction parameters (viz., reactants, pH, and temperature) was investigated. The binding constants were also determined (KA for [Cu(II)-His]+ and KB for ninhydrin). The resulting kψ-[16-s-16] plot can be understood in terms of a pseudo-phase model of micelles.

Although many compounds look similar to this compound(111-24-0)Related Products of 111-24-0, numerous studies have shown that this compound(SMILES:BrCCCCCBr), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis