Catalog Number |
ACM40000202 |
CAS |
40000-20-2 |
Structure |
![{[CurrentData.Name]}](https://resource.alfa-chemistry.com/structure/40000-20-2.gif) |
Description |
5-Bromo-1,10-phenanthroline (5-Br-Phen) is a commonly used organic compound with a wide range of applications in scientific research. It is a heterocyclic aromatic compound containing both a bromine atom and a phenanthroline ring. 5-Br-Phen has been used in the synthesis of a variety of organic compounds, and its unique properties have made it a valuable tool in the study of a variety of biochemical and physiological processes. |
Synonyms |
1,10-Phenanthroline, 5-bromo- |
IUPAC Name |
5-bromo-1,10-phenanthroline |
Molecular Weight |
259.1 g/mol |
Molecular Formula |
C12H7BrN2 |
Canonical SMILES |
C1=CC2=CC(=C3C=CC=NC3=C2N=C1)Br |
InChI |
InChI=1S/C12H7BrN2/c13-10-7-8-3-1-5-14-11(8)12-9(10)4-2-6-15-12/h1-7H |
InChI Key |
GWKGPQCKIBRXGW-UHFFFAOYSA-N |
Boiling Point |
417.6±25.0 °C(Predicted) |
Melting Point |
119 °C-lit. |
Purity |
97% |
Application |
5-Bromo-1,10-phenanthroline has a wide range of applications in scientific research. It has been used as a fluorescent probe for the detection of metal ions in aqueous solutions, and as a reagent for the synthesis of organic compounds. It has also been used to study the structure and properties of biological systems, such as proteins and DNA. In addition, 5-Bromo-1,10-phenanthroline has been used in the study of enzyme-catalyzed reactions, and as an inhibitor of various enzymes. |
Complexity |
234 |
Covalently-Bonded Unit Count |
1 |
EC Number |
254-742-7 |
Exact Mass |
257.97926 |
Heavy Atom Count |
15 |
Hydrogen Bond Acceptor Count |
2 |
Hydrogen Bond Donor Count |
0 |
Monoisotopic Mass |
257.97926 |
Properties |
5-Bromo-1,10-phenanthroline has been shown to have a variety of biochemical and physiological effects. It has been used to study the structure and properties of proteins and DNA, and has been used as an inhibitor of various enzymes. In addition, 5-Bromo-1,10-phenanthroline has been used in the study of enzyme-catalyzed reactions, and has been used as a fluorescent probe for the detection of metal ions in aqueous solutions. |
Rotatable Bond Count |
0 |
Topological Polar Surface Area |
25.8 Ų |