156492-30-7 | 4,7-Dibromo-1,10-phenanthroline

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$15.00	$11.00
250mg	97%	in stock	$36.00	$25.00
1g	97%	in stock	$100.00	$70.00
5g	97%	in stock	$448.00	$314.00

Description

• Catalog Number: AA78532
• Chemical Name: 4,7-Dibromo-1,10-phenanthroline
• CAS Number: 156492-30-7
• Molecular Formula: C12H6Br2N2
• Molecular Weight: 337.9974
• MDL Number: MFCD25562940
• SMILES: Brc1ccnc2c1ccc1c2nccc1Br

Computed Properties

• Complexity: 235
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 3.8

Upstream Synthesis Route

4,7-Dibromo-1,10-phenanthroline is a versatile chemical compound that finds wide application in chemical synthesis due to its unique properties. In organic chemistry, it serves as a highly efficient chelating agent and ligand in coordination complexes, displaying strong affinity for metal ions such as copper, palladium, and platinum. This makes it a valuable tool in catalytic reactions, particularly in cross-coupling reactions and other metal-mediated transformations.Furthermore, 4,7-Dibromo-1,10-phenanthroline is known for its ability to facilitate redox processes, making it useful in electrochemical studies and as a mediator in organic electrosynthesis. Its rigid molecular structure and electron-donating bromine substituents contribute to its stability and reactivity in various environments, allowing for controlled and selective reactions in complex molecular systems.Additionally, this compound is employed in the development of fluorescent probes and sensors for metal ions, owing to its fluorescent properties and metal-binding capabilities. By incorporating 4,7-Dibromo-1,10-phenanthroline into molecular designs, researchers can create sensitive and selective detection systems for monitoring metal ion concentrations in biological and environmental samples.Overall, the versatile nature of 4,7-Dibromo-1,10-phenanthroline makes it an indispensable tool in chemical synthesis, enabling researchers to explore new reaction pathways, design novel materials, and advance the field of coordination chemistry.

Literature

• Synthesis and characterization of a heteroleptic Ru(II) complex of phenanthroline containing oligo-anthracenyl carboxylic acid moieties.

  International journal of molecular sciences 20100101