Interesting facts
Interesting Facts about 1,4-Diphenylbenzene
1,4-Diphenylbenzene, also known as p-terphenyl, is a fascinating organic compound that has captivated the attention of chemists for various reasons. Here are some intriguing insights:
- Structure and Symmetry: The compound features a unique structure with three benzene rings connected in a linear fashion, creating a strong symmetry that contributes to its interesting properties.
- Applications in Science: 1,4-Diphenylbenzene is notably used in the field of organic chemistry and materials science. It serves as a model compound for studying p-conjugated systems and is appreciated for its role in photoconductive materials.
- Thermal Properties: This compound exhibits exceptional thermal stability, making it an ideal candidate for high-temperature applications. It is often employed in processes where heat resistance is crucial.
- Role in Organic Synthesis: In synthetic chemistry, 1,4-diphenylbenzene is utilized as a reagent and can be involved in various coupling reactions, enhancing its utility in laboratory settings.
- Research Potential: Ongoing research into this compound explores its potential applications in molecular electronics and as a component in organic light-emitting diodes (OLEDs), showcasing its versatility in modern technology.
In summary, 1,4-diphenylbenzene stands out for its unique structure, impressive thermal stability, and wide-ranging applications in both science and technology. As the field of chemistry continues to evolve, this compound remains a subject of great interest and ongoing study.
Synonyms
p-Terphenyl
92-94-4
1,4-Diphenylbenzene
1,1':4',1''-TERPHENYL
p-Diphenylbenzene
p-Triphenyl
4-Phenylbiphenyl
para-terphenyl
TERPHENYL
4-Phenyldiphenyl
Biphenyl, 4-phenyl-
1,1'-Biphenyl, 4-phenyl-
4-phenyl-1,1'-biphenyl
NSC 6810
PTP
MFCD00003061
GWP218ZY6F
CHEMBL491582
DTXSID6029121
CHEBI:52242
NSC-6810
p-Terphenyl (purified by sublimation)
Pyrogallol tannin
Tannin from pyrogallol
p-Terphenyl suitable for scintillation
CCRIS 1657
HSDB 5280
EINECS 202-205-2
UNII-GWP218ZY6F
triphenyl-
AI3-00847
PPP (scintillator)
TANNIN PYROGALLOL
TERPHENYL, P-
P-PHENYLENE TRIMER
WLN: RR DR
1,1':4',1"-Terphenyl
DTXCID907888
p-Terphenyl, analytical standard
NSC6810
Tox21_202759
BDBM50260180
MSK001314
p-Terphenyl, >=99.5% (HPLC)
STL069547
AKOS005111366
1,1'':4'',1''''-Terphenyl
CS-W014689
FD34319
CAS-92-94-4
NCGC00164113-01
NCGC00260306-01
AC-18695
AS-12803
1ST001314
DB-038209
MSK001314-1000
NS00003485
T0020
T3263
EN300-21317
p-Terphenyl Solution in Acetone, 1000?g/mL
p-Terphenyl Solution in Acetone, 1000mug/mL
D92686
T-3203
1ST001314-1000
AB-131/40897106
Q20965188
F0486-1779
Z104495322
p-Terphenyl, suitable for scintillation, >=98.5% (HPLC)
InChI=1/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14
Solubility of 1,4-Diphenylbenzene
1,4-Diphenylbenzene, with the chemical formula C12H10, is known for its unique structural characteristics that impact its solubility. Its solubility profile can be summarized as follows:
The interactions of 1,4-diphenylbenzene with organic solvents are influenced by van der Waals forces, providing a clear understanding of its behavior in different environments. This compound is a fascinating example of how molecular structure dictates solubility properties, emphasizing the importance of chemical characteristics in solubility studies.