Catalog Number |
ACM796966159 |
CAS |
796966-15-9 |
Structure |
![{[CurrentData.Name]}](https://resource.alfa-chemistry.com/structure/796966-15-9.gif) |
Description |
(1R,4R)-2,5-Diphenylbicyclo[2.2.2]octa-2,5-diene, also known as (1R,4R)-2,5-diphenylbicyclo[2.2.2]octa-2,5-diene, is an organic compound commonly used in synthetic organic chemistry. It is composed of two phenyl rings that are fused together, forming a bicyclic structure. This compound has been studied extensively in recent years due to its potential applications in synthetic organic chemistry, medicinal chemistry, and biochemistry. |
Synonyms |
Bicyclo[2.2.2]octa-2,5-diene, 2,5-diphenyl-, (1R,4R)- |
IUPAC Name |
(1R,4R)-2,5-diphenylbicyclo[2.2.2]octa-2,5-diene |
Molecular Weight |
258.4 g/mol |
Molecular Formula |
C20H18 |
Canonical SMILES |
C1CC2C=C(C1C=C2C3=CC=CC=C3)C4=CC=CC=C4 |
InChI |
InChI=1S/C20H18/c1-3-7-15(8-4-1)19-13-18-12-11-17(19)14-20(18)16-9-5-2-6-10-16/h1-10,13-14,17-18H,11-12H2/t17-,18-/m1/s1 |
InChI Key |
BDYBOFJAEBJDMI-QZTJIDSGSA-N |
Purity |
97% |
Application |
(1R,4R)-2,5-Diphenylbicyclo[2.2.2]octa-2,5-diene has been used in a variety of scientific research applications. For example, it has been used to synthesize a variety of organic compounds, such as heterocyclic compounds and polymers. It has also been used to study the mechanism of action of various drugs and to develop new drugs. Additionally, it has been used to study the structure-activity relationship of various compounds, as well as to synthesize new materials for use in various fields, such as electronics and biochemistry. |
GHS Pictogram |
Irritant; Environmental Hazard |
Isomeric SMILES |
C1C[C@@H]2C=C([C@H]1C=C2C3=CC=CC=C3)C4=CC=CC=C4 |
Properties |
The biochemical and physiological effects of (1R,4R)-2,5-diphenylbicyclo[2.2.2]octa-2,5-diene are not well understood. However, it is believed to be non-toxic and non-carcinogenic. Additionally, there is no evidence that this compound has any adverse effects on the environment. |