| Catalog Number |
ACM74866287-1 |
| CAS |
74866-28-7 |
| Structure |
 |
| Description |
2,2'-Dibromo-1,1'-binaphthyl (DBN) is a brominated organic compound belonging to the binaphthyl family. It is used as a reagent for a variety of organic syntheses, and as a chromophore for fluorescence applications. In addition, DBN has been studied for its potential applications in biochemistry and physiology. This paper will discuss the synthesis method, scientific research applications, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions for DBN. |
| IUPAC Name |
2-bromo-1-(2-bromonaphthalen-1-yl)naphthalene |
| Molecular Weight |
412.1 g/mol |
| Molecular Formula |
C20H12Br2 |
| Canonical SMILES |
C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)Br)Br |
| InChI |
InChI=1S/C20H12Br2/c21-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)22/h1-12H |
| InChI Key |
IJUDEFZBMMRSNM-UHFFFAOYSA-N |
| Application |
2,2'-Dibromo-1,1'-binaphthyl has been studied for its potential applications in a variety of scientific research areas. It has been used as a fluorescent tracer for studying the kinetics of enzyme-catalyzed reactions, and as a fluorescent probe for studying the structure and dynamics of proteins and other biomolecules. In addition, 2,2'-Dibromo-1,1'-binaphthyl has been used to study the structure and dynamics of DNA, as well as to study the binding of ligands to proteins. |
| GHS Pictogram |
Irritant |
| Properties |
The biochemical and physiological effects of 2,2'-Dibromo-1,1'-binaphthyl are not fully understood. However, it has been suggested that 2,2'-Dibromo-1,1'-binaphthyl may be involved in the regulation of gene expression. In addition, 2,2'-Dibromo-1,1'-binaphthyl has been studied for its potential applications in drug delivery, as a fluorescent probe for imaging, and as a fluorescent tracer for studying enzyme-catalyzed reactions. |
