774-53-8

Basic information

• Product Name: 5-BROMO-[2,3']-BIPYRIDINE
• Synonyms: 5-BROMO-[2,3']-BIPYRIDINE;5-bromo-2-(3-pyridyl)pyridine;3-Bromo-6-(3-pyridyl)pyridine;5-bromo-2-pyridin-3-ylpyridine
• CAS NO: 774-53-8
• Molecular Formula: C₁₀H₇BrN₂
• Molecular Weight: 235.07998
• Product Categories: Heterocyclic Compounds
• Mol File: 774-53-8.mol
• Article Data: 15

Chemical Properties

• Melting Point: 75-78°C
• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 5-BROMO-[2,3']-BIPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-[2,3']-BIPYRIDINE(774-53-8)
• EPA Substance Registry System: 5-BROMO-[2,3']-BIPYRIDINE(774-53-8)

Safety Data

• Hazardous Substances Data: 774-53-8(Hazardous Substances Data)

Usage

General Description

5-Bromo-[2,3']-bipyridine is a chemical compound with the molecular formula C10H7BrN2. It is a bipyridine derivative with a bromine atom at the 5-position of one of the pyridine rings. 5-BROMO-[2,3']-BIPYRIDINE is commonly used as a building block in the synthesis of coordination complexes, particularly in the field of coordination chemistry. Its unique structure and reactivity make it a valuable reagent for the preparation of various metal complexes, which have potential applications in catalysis, material science, and medicinal chemistry. Additionally, 5-Bromo-[2,3']-bipyridine is known for its fluorescence properties, which have led to its use in the development of fluorescent sensors and probes for analytical and bioimaging applications.

Upstream product

• 624-28-2 2,5-dibromopyridine 
• 89878-14-8 3-Diethylboranylpyridine 
• 626-55-1 3-Bromopyridine 
• 223463-13-6 2-iodo-5-bromopyridine 
• 1692-25-7 3-pyridylboronic acid 
• 220565-63-9 pyridin-3-ylzinc(II) bromide 

Downstream Products

• 1061149-87-8 5-p-tolyl-2,3'-bipyridine 
• 1314250-31-1 3-(2,3'-bipyridin-5-yl)aniline 
• 1314250-29-7 5-(4-methoxyphenyl)-2,3'-bipyridine 
• 1314250-33-3 methyl 4-(2,3'-bipyridin-5-yl)benzoate 
• 1264516-07-5 [2,3'-bipyridin]-5-ylboronic acid 
• 254902-22-2 2-(3-pyridyl)-5-[6-(3-pyridyl)-3-pyridyl]pyridine 
• 1260106-29-3 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3'-bipyridine 

Relevant articles and documents

Synthesis of Pyridoclax Analogues: Insight into Their Druggability by Investigating Their Physicochemical Properties and Interactions with Membranes

Pyridoclax is considered a promising anticancer drug, acting as a protein-protein interaction disruptor, with potential applications in the treatment of ovarian, lung, and mesothelioma cancers. Eighteen sensibly selected structural analogues of Pyridoclax

Compound containing quinoxaline and pyridine groups and organic electroluminescent device thereof

The invention provides an organic electroluminescent compound containing quinoxaline and pyridine groups. The compound has better heat stability, high luminous efficiency and high luminous purity, can be used for manufacturing an organic electroluminescent device, and is applied to the field of organic solar cells, organic thin film transistors or organic photoreceptors. The invention also provides the organic electroluminescent device, which comprises an anode, a cathode and an organic layer, wherein the organic layer includes more than one layer in a luminous layer, a hole injection layer, a hole transporting layer, a hole blocking layer, and electron injection layer and an electron transporting layer; at least one layer in the organic layer contains a compound as shown by a structural formula I which is as shown in the description.

Molecular design of high-molecular-orientation electron-transport materials and application to organic light-emitting diodes

Two novel electron-transport materials (ETMs), 2,3′-Bpy- TP and 2,4′-Bpy-TP, with high horizontal molecular orientation to substrates, were synthesized. It was shown by measuring the IR absorption spectra of their deposited thin films that C-H N hydrogen bonds are formed between the 2,3′-Bpy-TP molecules and between the 2,4′-Bpy-TP molecules. It was also shown that there is a closed relationship between their molecular orientations and the driving voltages of electron-only devices (EODs) using them as electron-transport layers (ETLs).