Pyridine is colorless, but older or impure samples can appear yellow. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. Historically, pyridine was produced from coal tar. Product Details of C6H6BrN.
Waters, Jessica E.;Hanf, Schirin;Rincon-Nocito, Marina;Bond, Andrew D.;Garcia-Rodriguez, Raul;Wright, Dominic S.;Colebatch, Annie L. research published 《 Synthesis and coordination behavior of aluminate-based quinolyl ligands》, the research content is summarized as follows. Lithium tris-quinolinylaluminate complexes were prepared by transmetalation of quinolinyllithium compounds with EtAlCl2; the electronic and steric effects of substitution of 2-quinolinyl groups for remote 8-quinolinyl groups were evaluated by single-crystal x-ray diffraction anal. and theor. calculations The effects of moving the donor N-atom from the 2-position in lithium (2-pyridyl)- and (2-quinolyl)aluminates to the more remote position in (8-quinolyl)aluminates have been investigated by solid-state structural and DFT computational studies of the new complexes [{EtAl(2-qy)3}Li(μ-X)Li(THF)3] (X = Cl/Br 62:38) [(1)Li(μ-X)Li(THF)3], [{(EtAl(2-qy)3)Li}2(μ-Br)]–Li(THF)4+ [{1Li}2(μ-Br)]–Li(THF)4+, [{EtAl(2-Me-8-qy)3}Li] [(2)Li], [{Me2Al(2-Me-8-qy)2}Li(THF)] [(3a)Li(THF)], [{Me2Al(6-Me-2-py)2}Li(THF)2] [(4)Li(THF)2] and [{{EtAl(2-Me-8-qy)2}2O}(Li2THF)] (5). Increasing the remoteness of the donor N-atom from the bridgehead results in large differences in the coordination of the Li+ cations by the (8-quinolyl)aluminate anions compared to 2-quinolyl or 2-pyridyl counterparts. The results are of potential interest in understanding how the coordination sites of ligands of this type can be tuned for the coordination requirements of specific metal centers.
5315-25-3, 2-Bromo-6-methylpyridine (2BMPy) is a bromopyridine derivative. It is formed when 2-chloro-6-methylpyridine is heated with bromotrimethylsilane. Its synthesis from various methods have been reported.
2-Bromo-6-methylpyridine is a building block in the preparation of nitrogen containing heterocyclic compounds.
2-Bromo-6-methylpyridine is an organic compound that belongs to the group of pyridinium halides. It is soluble in common solvents such as water, ethanol, and acetone. 2BMPy has been shown to act as a glutamate receptor antagonist and has been used in the study of glutamate receptors, including their subtypes. This chemical has also been shown to have antioxidant properties and can be used in the prevention of atherosclerosis., Product Details of C6H6BrN