Interesting facts
Interesting Facts about Tritylbenzene
Tritylbenzene is an intriguing chemical compound that captures the interest of chemists for various reasons. It is known for its unique structure and applications, making it a subject of study in both organic chemistry and materials science.
Key Characteristics
- Structure: Tritylbenzene comprises a benzene ring with three trityl groups attached. This complex configuration contributes to its stable properties.
- Synthesis: The synthesis of tritylbenzene can involve several synthetic routes, typically utilizing Friedel-Crafts alkylation, which highlights its importance in synthetic organic chemistry.
- Polyfunctional Reactivity: Due to its multiple reactive sites, tritylbenzene can undergo various chemical transformations. It serves as a versatile building block in organic synthesis.
Applications
- Organic Synthesis: As a multifunctional reagent, tritylbenzene aids in constructing more complex organic molecules.
- Research Tool: Scientists utilize tritylbenzene in studying reaction mechanisms due to its distinctive chemical behavior.
- Material Science: The compound's unique properties make it of interest in developing novel materials and enhancing performance in certain applications.
Fun Fact
Did you know that tritylbenzene has a connection to the fascinating world of polymers? Its derivatives are often explored for their potential use in high-performance materials due to their stability and reactivity.
In summary, tritylbenzene represents a fascinating intersection of structure, synthesis, and application in the chemical world, making it a notable compound for students and researchers alike.
Synonyms
Tetraphenylmethane
630-76-2
Tritylbenzene
METHANE, TETRAPHENYL-
Tetraphenyl methane
EINECS 211-144-0
NSC 43332
BRN 1913557
CM2Q9C446P
NSC-43332
Benzene, 1,1',1'',1'''-methanethetrayltetrakis-
1,1',1'',1'''-methanetetrayltetrabenzene
DTXSID30212215
4-05-00-02741 (Beilstein Handbook Reference)
1,1',1'',1'''-Methanetetrayltetrakis[benzene]
1,1',1'',1'''-Methanetetrayltetrakis(benzene)
DTXCID30134706
211-144-0
inchi=1/c25h20/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20
peqhirfakiasbk-uhfffaoysa-n
Benzene, 1,1',1'',1'''-methanetetrayltetrakis-
MFCD00014428
C25H20
Tritylbenzene #
Tetraphenylmethane, 97%
UNII-CM2Q9C446P
YSZC012
BCP10895
NSC43332
BBL103381
STL557191
AKOS005259872
CS-W009895
AS-15832
SY037712
DB-054401
NS00041933
T0169
Benzene,1',1'',1'''-methanetetrayltetrakis-
F15495
10.14272/PEQHIRFAKIASBK-UHFFFAOYSA-N.1
10.14272/PEQHIRFAKIASBK-UHFFFAOYSA-N.2
Q420710
doi:10.14272/PEQHIRFAKIASBK-UHFFFAOYSA-N.1
doi:10.14272/PEQHIRFAKIASBK-UHFFFAOYSA-N.2
Solubility of Tritylbenzene
Tritylbenzene, with the molecular formula C19H18, exhibits particularly intriguing solubility characteristics that are worth noting. Being a hydrocarbon compound, its solubility behavior is primarily influenced by its non-polar nature.
Key Points on Solubility:
Due to these properties, tritylbenzene serves as a useful compound in organic synthesis where non-polar conditions are required.