178039-84-4

Basic information

• Product Name: 6-AMINO-2,2'-BIPYRIDINE
• Synonyms: 6-AMINO-2,2'-BIPYRIDINE;2,2-bipyridin-6-amine;6-pyridin-2-ylpyridin-2-amine;6-Amine-2,2'-bipyridin
• CAS NO: 178039-84-4
• Molecular Formula: C₁₀H₉N₃
• Molecular Weight: 171.20
• Mol File: 178039-84-4.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 364.688 °C at 760 mmHg
• Flash Point: 201.892 °C
• Appearance: /
• Density: 1.193 g/cm³
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 6-AMINO-2,2'-BIPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINO-2,2'-BIPYRIDINE(178039-84-4)
• EPA Substance Registry System: 6-AMINO-2,2'-BIPYRIDINE(178039-84-4)

Safety Data

• Hazardous Substances Data: 178039-84-4(Hazardous Substances Data)

Usage

General Description

6-Amino-2,2'-bipyridine is a chemical compound that consists of a bipyridine core with an amino group located at the 6-position. It is commonly used as a ligand in coordination chemistry, particularly in the synthesis of metal complexes. 6-AMINO-2,2'-BIPYRIDINE has a strong chelating ability, allowing it to form stable complexes with various metal ions, such as copper, nickel, and platinum. These complexes have been investigated for their potential applications in catalysis, materials science, and medicinal chemistry. Additionally, 6-amino-2,2'-bipyridine has been studied for its fluorescence properties, making it useful in the development of fluorescent sensors and probes for detecting metal ions in biological and environmental systems.

Upstream product

• 10495-73-5 2-bromo-6-(pyridin-2-yl)pyridine 
• 33421-43-1 2,2'-bipyridyl N-oxide 
• 75-64-9 tert-butylamine 
• 19798-81-3 2-Amino-6-bromopyridine 
• 882521-96-2 pyridine-2-boronic acid N-phenyldiethanolamine ester 
• 366-18-7 [2,2]bipyridinyl 
• 109-04-6 2-bromo-pyridine 
• 13040-77-2 6-Chloro-[2,2']bipyridinyl 
• 108-95-2 phenol 

Downstream Products

• 885622-40-2 [(6-amino-2,2'-bipyridine)(acetonitrile)platinum(II)methyl][B(3,5-(CF₃)2C₆H₃)4] 

Relevant articles and documents

Electrocatalytic carbon dioxide reduction by using cationic pentamethylcyclopentadienyl-iridium complexes with unsymmetrically substituted bipyridine ligands

Eight [Ir(bpy)CpCl]+-type complexes (bpy= bipyridine, Cp=1,2,3,4,5-pentamethylcyclopentadienyl) containing differently substituted bipyridine ligands were synthesized and characterized. Cyclic voltammetry (CV) of the complexes in Ar-saturated a

ZnCl2 Capture Promotes Ethylene Polymerization by a Salicylaldiminato Ni Complex Bearing a Pendent 2,2′-Bipyridine Group

The effect of ZnCl2 additives on a series of (salicylaldiminato)Ni ethylene polymerization catalysts is reported. While ZnCl2 acts solely as a pyridine scavenger for simple imine catalyst frameworks such as the biphenylimine 4, in th

Synthesis, guest binding, and metal coordination of functionalized self-folding deep cavitands

A simple method to introduce donor functions to the upper rim of self-folding benzimidazole-based deep cavitands is described. The upper rim donors allow controlled noncovalent binding of suitably sized guest species via both self-complementary hydrogen bonding and space-filling interactions, and metal-mediated self-folding is possible if bidentate coordinators are incorporated.