871507-79-8

Basic information

• Product Name: 2,8-Dibromoquinoline
• Synonyms: 2,8-Dibromoquinoline;Quinoline, 2,8-dibroMo-
• CAS NO: 871507-79-8
• Molecular Formula: C₉H₅Br₂N
• Molecular Weight: 286.953
• Mol File: 871507-79-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 118-119 °C
• Boiling Point: 349.4±22.0 °C(Predicted)
• Appearance: /
• Density: 1.923±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: -2.16±0.50(Predicted)
• CAS DataBase Reference: 2,8-Dibromoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2,8-Dibromoquinoline(871507-79-8)
• EPA Substance Registry System: 2,8-Dibromoquinoline(871507-79-8)

Safety Data

• Hazardous Substances Data: 871507-79-8(Hazardous Substances Data)

Usage

General Description

2,8-Dibromoquinoline is a chemical compound with the molecular formula C9H5Br2N. It is a member of the quinoline family, which is a class of aromatic organic compounds. 2,8-Dibromoquinoline is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. It is primarily used in the synthesis of pharmaceuticals and agrochemicals. 2,8-Dibromoquinoline has also been studied for its potential biological activities, including its use as an antifungal agent. Additionally, it has been investigated for its potential applications in organic electronic devices due to its unique electronic and optical properties. Nonetheless, more research is needed to fully understand its potential uses and properties.

Upstream product

• 67805-67-8 8-bromo-1H-quinoline-2-one 
• 615-36-1 2-bromoaniline 
• 71910-51-5 N-(2-bromophenyl)-3-phenylacrylamide 

Downstream Products

• 871507-80-1 8-bromo-2-phenylquinoline 
• 16032-40-9 2-(4-methoxyphenyl)quinoline 
• 1106785-14-1 8-bromo-2-(4-methoxyphenyl)quinoline 
• 61047-43-6 8-bromo-2-methylquinoline 
• 1463-17-8 2,8-dimethylquinoline 
• 1262757-99-2 2,8-bis(2-methoxymethoxy-3,5-di-tert-butylphenyl)quinoline 
• 1261135-27-6 8-bromo-2-(3,5-di-tert-butyl-2-methoxyphenyl)quinoline 
• 1258956-51-2 N-(2,6-dimethylphenyl)-2-(1-naphthyl)-8-quinolinamine 
• 1258956-52-3 N-(2,6-diisopropylphenyl)-2-(1-naphthyl)-8-quinolinamine 
• 1261135-32-3 2,4-di-tert-butyl-6-[8-(2,6-dimethylanilino)-2-quinolinyl]phenol 
• 1418268-29-7 N-(2,6-diisopropylphenyl)-2-phenyl-8-quinolinamine 
• 1418268-30-0 N-(2,6-diisopropylphenyl)-2-(4-tert-butylphenyl)-8-quinolinamine 
• 1418268-31-1 N-(2,6-diisopropylphenyl)-2-(4-methylphenyl)-8-quinolinamine 
• 1418268-32-2 N-(2,6-diisopropylphenyl)-2-(4-fluorophenyl)-8-quinolinamine 

Relevant articles and documents

New tridentate cyclometalated platinum(II) and palladium(II) complexes of N,2-diphenyl-8-quinolinamine: Syntheses, crystal structures, and photophysical properties

A new tridentate cyclometalated platinum(II) complex derived from N,2-diphenyl-8-quinolinamine, which consists of two crystallographic independent molecules with two intermolecular N-H-Cl-Pt hydrogen bonds forming a dimer, exhibited a low-energy luminesce

Iron Complexes of Square Planar Tetradentate Polypyridyl-Type Ligands as Catalysts for Water Oxidation

The tetradentate ligand, 2-(pyrid-2′-yl)-8-(1″,10″-phenanthrolin-2″-yl)-quinoline (ppq) embodies a quaterpyridine backbone but with the quinoline C8 providing an additional sp2 center separating the two bipyridine-like subunits. Thus, the four

IMIDAZO[1,2-A]PYRIDINE COMPOUNDS AS RECEPTOR TYROSINE KINASE INHIBITORS

Compounds of Formula I: in which A, B, R1, R1a, R2, R3, R4, R5 R6, R7 and R8 have the meanings given in the specification, are receptor tyrosine inhibitors useful in the treatment of diseases mediated by class 3 and class 5 receptor tyrosine kinases. Particular compounds of this invention have also been found to be inhibitors of Pim-1.