Interesting facts
Interesting Facts about 1,2-Diphenylvinylbenzene
1,2-diphenylvinylbenzene, often abbreviated as DPVB, is a fascinating compound that plays a significant role in various chemical applications. Here are some intriguing aspects of this compound:
- Structural Composition: This compound contains multiple benzene rings, making it an example of a polycyclic aromatic hydrocarbon. The presence of multiple phenyl groups contributes to its unique electronic properties.
- Polymerization Potential: DPVB is known for its ability to undergo polymerization reactions, which is valuable in the synthesis of new materials, particularly in the field of organic electronics.
- Light Absorption: One of the most notable features of DPVB is its capacity to absorb light in the ultraviolet region. This characteristic makes it useful in photonic applications and as a potential photoinitiator in polymer chemistry.
- Applications: Beyond basic research, 1,2-diphenylvinylbenzene is utilized in the production of liquid crystals and organic solar cells, highlighting its importance in modern technology.
- Research Dynamics: The study of DPVB has inspired numerous research articles focusing on its electronic properties, interactions in various solvents, and potential applications in organic synthesis.
In the words of chemical researchers, "The exploration of polycyclic compounds like 1,2-diphenylvinylbenzene opens new horizons in material science, making it a cornerstone of innovation." This compound continues to intrigue scientists due to its versatile properties and promising applications in various fields.
Whether you're a chemistry student or a seasoned scientist, understanding the complexities of 1,2-diphenylvinylbenzene is essential for anyone interested in the forefront of chemical research and technology.
Synonyms
TRIPHENYLETHYLENE
58-72-0
Triphenylethene
1,1,2-Triphenylethylene
Ethylene, triphenyl-
1,2-diphenylethenylbenzene
Benzilidenediphenylmethane
1,2,2-Triphenylethylene
(1,2-Diphenylvinyl)benzene
Benzene, 1,1',1''-(1-ethenyl-2-ylidene)tris-
1,2-diphenylvinylbenzene
UNII-S4ZLZ1K74B
EINECS 200-395-1
S4ZLZ1K74B
MFCD00004765
NSC 17535
(1,2-diphenylethenyl)benzene
DTXSID3022320
1,1,2-triphenylethene
NSC-17535
DTXCID402320
CHEBI:35034
Ethene-1,1,2-triyltribenzene
NSC17535
(2,2-diphenylethenyl)benzene
triphenyl-ethene
Ethylene, triphenyl
1,2-Triphenylethylene
1,1,2Triphenylethylene
1,2,2Triphenylethylene
Triphenylethylene, 99%
BIDD:ER0166
(1,2-Diphenylvinyl)benzene #
CHEMBL3115201
Tox21_302425
AKOS015903680
HY-W150752
CAS-58-72-0
NCGC00255197-01
AC-10375
AS-13154
SY048481
1,1',1''-ethene-1,1,2-triyltribenzene
Benzene, 1,1',1''(1ethenyl2ylidene)tris
CS-0207226
NS00005389
T1834
Benzene,1',1''-(1-ethenyl-2-ylidene)tris-
AB-016/30004060
Q25100760
200-395-1
Solubility of 1,2-diphenylvinylbenzene (C26H20)
1,2-diphenylvinylbenzene is a complex aromatic hydrocarbon that exhibits unique solubility characteristics. Its solubility can be predominantly influenced by the following factors:
It is noteworthy that this compound is practically insoluble in water due to the polar nature of water molecules that are unable to interact effectively with the compound’s hydrophobic structure. Instead, it readily dissolves in:
In summary, one can conclude that the solubility of 1,2-diphenylvinylbenzene is primarily limited to non-polar organic solvents, reflecting its hydrophobic characteristics while being significantly insoluble in polar solvents such as water.