1803458-54-9 Usage
Unique structure
2,3,6,7,12,13-hexaphenyltriptycene has a distinct structure that consists of six phenyl groups attached to a triptycene core.
Polycyclic aromatic hydrocarbon
This chemical compound is a polycyclic aromatic hydrocarbon, which means it is composed of multiple aromatic rings.
Rigid and planar structure
The structure of 2,3,6,7,12,13-hexaphenyltriptycene is rigid and planar, making it useful in materials science and organic electronics.
Stable and highly ordered molecular assemblies
2,3,6,7,12,13-hexaphenyltriptycene has been studied for its ability to form stable and highly ordered molecular assemblies, which makes it useful for creating novel nanomaterials with tailored electronic and optical properties.
Aromatic nature
The aromatic nature of 2,3,6,7,12,13-hexaphenyltriptycene, combined with its large π-conjugated system, makes it a promising candidate for applications in organic semiconductors and optoelectronic devices.
Building block for advanced materials
2,3,6,7,12,13-hexaphenyltriptycene shows promise as a building block for the design and synthesis of advanced materials for various technological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1803458-54-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,0,3,4,5 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1803458-54:
(9*1)+(8*8)+(7*0)+(6*3)+(5*4)+(4*5)+(3*8)+(2*5)+(1*4)=169
169 % 10 = 9
So 1803458-54-9 is a valid CAS Registry Number.
1803458-54-9Relevant articles and documents
Synthesis of Triphenylene-Based Triptycenes via Suzuki-Miyaura Cross-Coupling and Subsequent Scholl Reaction
Reinhard, Dennis,Rominger, Frank,Mastalerz, Michael
, p. 9342 - 9348 (2015)
A two-step method (Suzuki-Miyaura cross-coupling, followed by Scholl oxidation) to triphenylene-based triptycenes is described, rendering a variety of -extended triptycenes accessible in high yields and without the necessity of column chromatography purif
