117330-41-3

Basic information

• Product Name: 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate
• Synonyms: 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate
• CAS NO: 117330-41-3
• Molecular Weight: 458.106
• Mol File: 117330-41-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate(117330-41-3)
• EPA Substance Registry System: 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate(117330-41-3)

Safety Data

• Hazardous Substances Data: 117330-41-3(Hazardous Substances Data)

Upstream product

• 144342-49-4 6,6′-dimethyl-2,2′-bipyridine-4,4′-dicarboxylic acid 
• 144342-48-3 4,4'-Bis(fur-2-yl)-6,6'-dimethyl-2,2'-bipyridine 
• 92152-08-4 (1E,5E)-1,6-di(furan-2-yl)hexa-1,5-diene-3,4-dione 
• 562086-28-6 methyl 2-methyl-6-<(p-toluenesulfonyl)oxy>pyridine-4-carboxylate 
• 98491-78-2 methyl 6-methyl-2-hydroxypyridine-4-carboxylate 
• 117330-40-2 dimethyl 6,6'-dimethyl-2,2'-bipyridine-4,4'-dicarboxylate 

Downstream Products

• 381224-19-7 C₅₀H₅₀N₆O₁₂S₂ 

Relevant articles and documents

Practical bromination approach to the synthesis of dimethyl 6,6’-bis(Bromomethyl)-[2,2’-bipyridine]-4,4’-dicarboxylate

Dimethyl 6,6’-bis(bromomethyl)-[2,2’-bipyridine]-4,4’-dicarboxylate (2) was synthesized from dimethyl 6,6’-dimethyl-2,2'-bipyridine-4,4'-dicarboxylate (1) through dibromination and debromination. Debromination of dimethyl 6,6’-bis(dibromomethyl)-[2,2’-bip

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.