144342-48-3

Basic information

• Product Name: 2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethyl-
• CAS NO: 144342-48-3
• Molecular Formula: C20H16N2O2
• Mol File: 144342-48-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethyl-(144342-48-3)
• EPA Substance Registry System: 2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethyl-(144342-48-3)

Safety Data

• Hazardous Substances Data: 144342-48-3(Hazardous Substances Data)

Usage

General Description

2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethyl- is a chemical compound with two important molecular components. The first component is 2,2'-bipyridine, which is a nitrogen-containing heterocyclic compound commonly used as a chelating ligand in coordination chemistry. It is known for its ability to form stable complexes with a variety of metal ions. The second component is 4,4'-di-2-furanyl-6,6'-dimethyl-, which is a derivative of furan, a heterocyclic compound containing an oxygen atom in its ring structure. 2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethyl- is known for its unique furan ring and has potential applications in organic synthesis and material science. When combined, these two components create a complex molecule with potential applications in coordination chemistry and organic synthesis.

Upstream product

• 92152-08-4 1,6-di-furan-2-yl-hexa-1,5-diene-3,4-dione 
• 17282-41-6 N-acetonylpyridinium bromide 
• 92152-08-4 (1E,5E)-1,6-di(furan-2-yl)hexa-1,5-diene-3,4-dione 
• 42508-60-1 1-(2-oxopropyl)pyridinium chloride 

Downstream Products

• 117330-40-2 dimethyl 6,6'-dimethyl-2,2'-bipyridine-4,4'-dicarboxylate 
• 117330-41-3 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate 
• 144342-49-4 6,6′-dimethyl-2,2′-bipyridine-4,4′-dicarboxylic acid 

Relevant articles and documents

Lanthanide-series compound and preparation method and application thereof

The invention provides a lanthanide-series compound and a preparation method and an application thereof; the lanthanide-series compound has the chemical structural formula described in the description. The lanthanide-series compound has no inversion center, is beneficial for the compound to generate higher-brightness fluorescence, and enables a strongest emission peak to be used in a fluorescence analysis peak of time-resolved fluorescence immunoassay; and at the same time, the compound has relatively strong stability, and still can be used for marking and testing after being placed for a certain time.