Interesting facts
Interesting Facts about 1,3,5-Triphenylbenzene
1,3,5-Triphenylbenzene is a fascinating aromatic hydrocarbon that serves as an intriguing subject of study in the field of organic chemistry. Here are some compelling points about this compound:
- Structure and Symmetry: The compound features a unique triphenyl structure where three phenyl groups are symmetrically attached to a central benzene ring. This symmetry contributes to its interesting chemical and physical properties.
- Optical and Electronic Properties: Due to its highly conjugated π-system, 1,3,5-triphenylbenzene exhibits notable optical and electronic characteristics. It has potential applications in the field of organic electronics, such as in organic light-emitting diodes (OLEDs).
- Application in Material Science: This compound is of particular interest for researchers exploring new materials. Its structure allows for the possibility of forming ordered arrangements, leading to interesting insights in the realm of crystalline materials.
- Research Relevance: As a derivative of benzene, 1,3,5-triphenylbenzene is often studied in relation to other polycyclic aromatic hydrocarbons (PAHs). Its study can lead to a better understanding of the reactivity and interactions of such compounds.
- Chemical Synthesis: The synthesis of this compound can involve multiple methods, including coupling reactions. Its preparation is a great example of how chemists can manipulate molecular structures to achieve desired outcomes.
In summary, 1,3,5-triphenylbenzene not only showcases the beauty of organic structures but also paves the way for advancements in various scientific domains. As quoted by renowned chemist Linus Pauling, "Chemistry is the shaping of molecules," and in the case of 1,3,5-triphenylbenzene, we see this shaping leading to diverse opportunities for discovery and innovation.
Synonyms
1,3,5-Triphenylbenzene
612-71-5
5'-Phenyl-1,1':3',1''-terphenyl
Triphenylbenzene
s-Triphenylbenzene
5'-Phenyl-m-terphenyl
m-Terphenyl, 5'-phenyl-
1,1':3',1''-Terphenyl, 5'-phenyl-
Benzene, 1,3,5-triphenyl-
1,1'-Biphenyl, 3,5-diphenyl-
NSC 17358
EINECS 210-318-3
UNII-408MSO5WO3
BRN 1912744
408MSO5WO3
AI3-02595
NSC-17358
Symmetrical triphenylbenzene
DTXSID9073917
4-05-00-02732 (Beilstein Handbook Reference)
sTriphenylbenzene
5'Phenylmterphenyl
mTerphenyl, 5'phenyl
Benzene, 1,3,5triphenyl
1,1'Biphenyl, 3,5diphenyl
DTXCID7042986
1,1':3',1''Terphenyl, 5'phenyl
1,1':3',1''-Terphenyl, 5'-phenyl-(9CI)
210-318-3
inchi=1/c24h18/c1-4-10-19(11-5-1)22-16-23(20-12-6-2-7-13-20)18-24(17-22)21-14-8-3-9-15-21/h1-18
sxwiaeozzqadey-uhfffaoysa-n
MFCD00003060
1,3,5-Triphenylbenzene 10 microg/mL in Acetonitrile
NSC17358
1,5-Triphenylbenzene
1, 3,5-diphenyl-
Benzene,3,5-triphenyl-
WLN: RR CR ER
1,3,5-Triphenyl Benzene
YSWG254
1,3,5-Triphenylbenzene, 97%
1,1''-Terphenyl, 5'-phenyl-
AKOS015904072
3,5-DIPHENYL-1,1'-BIPHENYL
AC-13455
PS-11005
SY033595
CS-0111053
NS00034627
T0509
D70967
EN300-171705
Q27258308
Solubility of 1,3,5-Triphenylbenzene
1,3,5-Triphenylbenzene (C24H18) is a fascinating organic compound known for its unique structure and properties. When it comes to its solubility, here are some key points to consider:
In summary, the solubility of 1,3,5-triphenylbenzene is significantly influenced by the solvent used, with a clear preference for non-polar environments. As stated, "Like dissolves like," and this principle holds true for this compound.