The critical parameters of pyridine are pressure 6.70 MPa, temperature 620 K and volume 229 cm3·mol−1. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. In the temperature range 340–426 °C its vapor pressure p can be described with the Antoine equation.. COA of Formula: C6H6BrN.
Vanga, Mukundam;Lalancette, Roger A.;Jaekle, Frieder research published 《 Controlling the Optoelectronic Properties of Pyrene by Regioselective Lewis Base-Directed Electrophilic Aromatic Borylation》, the research content is summarized as follows. Pyreno-annelated azaboroles I (5, X = C13H27, R = Ph, Et) and azaborines II (6, Y = C8H17, R = Ph, Et) were prepared by stepwise borylation-Suzuki coupling of pyrene and examined for their photophys. properties. Given that pyrene represents one of the most versatile chromophores, the development of new selective routes for its functionalization and tuning of its emission properties is highly desirable. Pyrene-based BN Lewis pair (LP)-functionalized polycyclic aromatic hydrocarbons (PAHs) were prepared by regioselective Lewis base-directed electrophilic aromatic substitution. The requisite 1,6-dipyridylpyrene ligands were accessed by Suzuki-Miyaura cross-coupling of 1,6-bis(pinacolatoboryl)pyrenes with 2-bromopyridine derivatives Subsequent electrophilic borylation with BCl3 in the presence of AlCl3 and 2,6-di-tert-butylpyridine as a hindered base produced the dichloroborane complexes, which were then in situ reacted with di-Ph or di-Et zinc. The presence or absence of alkyl chains in the 3,8-positions of the pyrene moiety determined the position of the B-C bond formation (2,7 in the non-K region vs. 5,10 in the K region) and thereby also the size of the BN heterocycle (five- vs. six-membered). The impact of the regioisomeric borylation on the electrochem., photophys. and structural properties was investigated and the conclusions supported by theor. calculations The rapid synthesis of derivatives that are borylated in the K region also suggests strong potential for the development of pyrene derivatives that are otherwise difficult to access.
COA of Formula: C6H6BrN, 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., 5315-25-3.