129265-60-7

Basic information

• Product Name: 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)-
• CAS NO: 129265-60-7
• Molecular Formula: C24H14Br2N2
• Molecular Weight: 490.197
• Mol File: 129265-60-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)-(129265-60-7)
• EPA Substance Registry System: 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)-(129265-60-7)

Safety Data

• Hazardous Substances Data: 129265-60-7(Hazardous Substances Data)

Usage

Description

1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is a chemical compound that belongs to the phenanthroline family. It is a fluorescent dye used in analytical chemistry and biochemistry as a chelating agent for metal ions. 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is known for its ability to form stable complexes with transition metals, which has significant implications in various fields such as coordination chemistry, catalysis, and biological research. The derivative, 2,9-bis(4-bromophenyl)-1,10-phenanthroline, possesses specific properties that make it potentially useful in the development of new materials and technologies. Due to its versatile characteristics, 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is widely employed in scientific research and industrial applications.

Uses

Used in Analytical Chemistry:
1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is used as a chelating agent for metal ions in analytical chemistry. Its ability to form stable complexes with transition metals allows for the accurate detection and quantification of these metals in various samples.
Used in Biochemistry:
In biochemistry, 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is used as a fluorescent dye for the detection and analysis of metal ions. Its fluorescence properties enable researchers to study the interactions between metal ions and biomolecules, providing valuable insights into biological processes.
Used in Coordination Chemistry:
1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is used as a ligand in coordination chemistry to form complexes with transition metals. These complexes are essential for understanding the structure, properties, and reactivity of metal-containing compounds.
Used in Catalysis:
In the field of catalysis, 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is used to form metal complexes that act as catalysts in various chemical reactions. These catalysts play a crucial role in enhancing the efficiency and selectivity of the reactions.
Used in Biological Research:
1,10-Phenanthroline, 2,9-bis(4-bromophenyl)is used as a research tool in biological studies to investigate the role of metal ions in biological systems. Its ability to form stable complexes with transition metals helps researchers understand the mechanisms of metal ion interactions with biomolecules and their impact on cellular processes.
Used in the Development of New Materials and Technologies:
The specific properties of 1,10-Phenanthroline, 2,9-bis(4-bromophenyl)make it a valuable compound for the development of new materials and technologies. Its potential applications include the creation of advanced materials with unique properties, such as improved sensitivity in sensors or enhanced catalytic activity in chemical processes.

Upstream product

• 29176-55-4 2,9-dichloro-[1,10]phenanthroline 
• 106-37-6 1.4-dibromobenzene 
• 66-71-7 1,10-Phenanthroline 
• 149054-39-7 2-(4'-bromophenyl)-1,10-phenanthroline 
• 5467-74-3 4-Bromophenylboronic acid 
• 207461-15-2 2,9-diiodo-[1,10]phenanthroline 
• 1190590-49-8 2,9-bis(4-trimethylsilylphenyl)-1,10-phenanthroline 

Downstream Products

• 1190590-53-4 2,9-bis(4'-(4''-pyridyl)phenyl)-1,10-phenanthroline 
• 120086-02-4 C₁₄₈H₁₅₆N₁₀Zn₂ 
• 129265-63-0 2,9-Bis-(2'-bromomethyl-biphenyl-4-yl)-[1,10]phenanthroline 
• 129265-62-9 {4'-[9-(2'-Hydroxymethyl-biphenyl-4-yl)-[1,10]phenanthrolin-2-yl]-biphenyl-2-yl}-methanol 
• 830328-51-3 C₄₀H₂₈N₂O₄ 
• 540770-66-9 2,9-bis[4'-(4-pyridyl-4-phenoxy)biphenyl]-1,10-phenanthroline 
• 129265-61-8 2,9-bis-1,10-phenanthroline 

Relevant articles and documents

NOVEL COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE ELEMENT, ORGANIC ELECTROLUMINESCENCE ELEMENT, AND ELECTRONIC DEVICE

A compound is represented by a formula (1) below. In the formula (1), X1 to X8 each independently represent a carbon atom to be bonded to a group represented by a formula (20) below, CRX or a nitrogen atom. At least one of X1 to X8 is a carbon atom to be bonded to the group represented by the formula (2). RX is independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, and the like.

Phenanthroline ligands with divergent pyridine units

2-Mono- and 2,9-di-substituted 1,10-phenanthrolines with 4-pyridine units attached either via 1,4-phenylene- or 4-ethynyl-phenyl spacers, have been synthesised. The strategy is based on the introduction of 4-trimethylsilylphenyl group(s) at the phenanthro

Synthesis of unsymmetrical 2,8- and 2,9-dihalo-1,10-phenanthrolines and derivatives

A general method for the preparation of the unsymmetrical 2,8- and 2,9- dihalophenanthrolines is presented. The use of these halophenanthrolines as synthetic substrates in the Suzuki and Sonogashira/Castro-Stevens palladium catalyzed chemistry is exemplifed. The derivatized phenanthrolines are seen as key building blocks for the design and construction of topologically complex polynuclear metal coordination complexes.