| Catalog Number |
ACM76905801 |
| CAS |
76905-80-1 |
| Structure |
 |
| Description |
1,1'-Binaphthalene, 2,2'-diiodo-' (BNI) is an organic compound composed of two fused naphthalene rings with two iodine atoms attached to the 2-position of each naphthalene ring. It is an important building block for organic synthesis and has been used in a variety of scientific research applications. This paper will discuss the synthesis method, scientific research application, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions of BNI. |
| IUPAC Name |
2-iodo-1-(2-iodonaphthalen-1-yl)naphthalene |
| Molecular Weight |
506.1 g/mol |
| Molecular Formula |
C20H12I2 |
| Canonical SMILES |
C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)I)I |
| InChI |
InChI=1S/C20H12I2/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 |
KZSPPDFSBAVQBI-UHFFFAOYSA-N |
| Application |
1,1'-Binaphthalene, 2,2'-diiodo- has been used in a variety of scientific research applications. It has been used in the synthesis of organic compounds, such as 1,2,3-triiodobenzene, 1,2,4-triiodobenzene, and 1,2,3,4-tetraiodobenzene. It has also been used in the synthesis of heterocyclic compounds, such as 1,2,3-triazole and 1,2,3-triazine. Additionally, 1,1'-Binaphthalene, 2,2'-diiodo- has been used in the synthesis of polymers, such as poly(vinyl chloride) and poly(ethylene terephthalate). |
| Properties |
The biochemical and physiological effects of 1,1'-Binaphthalene, 2,2'-diiodo- are not well understood. However, it has been suggested that 1,1'-Binaphthalene, 2,2'-diiodo- may act as an antioxidant, which could have beneficial effects on the body. Additionally, 1,1'-Binaphthalene, 2,2'-diiodo- has been shown to have anti-inflammatory effects, which could be beneficial in treating certain conditions. |
