865604-20-2

Basic information

• Product Name: 3,4'-BIPYRIDIN-2'-AMINE
• Synonyms: [3,4'-bipyridin]-2'-amine; 3,4'-Bipyridin-2'-amine
• CAS NO: 865604-20-2
• Molecular Formula: C₁₀H₉N₃
• Molecular Weight: 171.2
• Mol File: 865604-20-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 371.9°C at 760 mmHg
• Flash Point: 206.5°C
• Appearance: /
• Density: 1.193g/cm³
• Vapor Pressure: 9.95E-06mmHg at 25°C
• Refractive Index: 1.633
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 3,4'-BIPYRIDIN-2'-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4'-BIPYRIDIN-2'-AMINE(865604-20-2)
• EPA Substance Registry System: 3,4'-BIPYRIDIN-2'-AMINE(865604-20-2)

Safety Data

• Statements: 41
• Safety Statements: 26-39
• Hazardous Substances Data: 865604-20-2(Hazardous Substances Data)

Usage

General Description

3,4'-Bipyridin-2'-amine, also known as 2-Amino-3,4'-bipyridine, is a chemical compound composed of two pyridine rings connected by a carbon-carbon bond at the 3 and 4 positions. It is classified as an aromatic amine and is commonly used in the synthesis of various organic compounds and pharmaceuticals. This chemical has been studied for its potential use in the development of new materials and pharmaceuticals due to its unique structural and reactivity properties. It is also known for its ability to form metal complexes, making it useful in the field of coordination chemistry. 3,4'-BIPYRIDIN-2'-AMINE is often used as a building block in organic synthesis and chemical research.

InChI:InChI=1/C10H9N3/c11-10-6-8(3-5-13-10)9-2-1-4-12-7-9/h1-7H,(H2,11,13)

Upstream product

• 19798-80-2 2-Amino-4-chloropyridine 
• 1692-25-7 3-pyridylboronic acid 
• 84249-14-9 2-amino-4-bromopyridine 

Downstream Products

• 1131410-80-4 C₁₇H₁₅N₃O₂S 

Relevant articles and documents

DNA gyrase (GyrB)/topoisomerase IV (ParE) inhibitors: Synthesis and antibacterial activity

The synthesis and antibacterial activities of three chemotypes of DNA supercoiling inhibitors based on imidazolo[1,2-a]pyridine and [1,2,4]triazolo[1,5-a]pyridine scaffolds that target the ATPase subunits of DNA gyrase and topoisomerase IV (GyrB/ParE) is reported. The most potent scaffold was selected for optimization leading to a series with potent Gram-positive antibacterial activity and a low resistance frequency.

New catalysts for Suzuki-Miyaura coupling reactions of heteroatom- substituted heteroaryl chlorides

(Chemical Equation Presented) The new air-stable PdCl2{PR 2(Ph-R′)}2 complexes, readily prepared from commercial reagents, exhibit unique efficiency as catalysts for the Suzuki-Miyaura coupling reactions of a variety of he