2230887-26-8 Usage
Uses
Used in Coordination Polymers and Metal-Organic Frameworks:
2,4,6-tris(4-formylphenyl)pyridine is used as a building block for the synthesis of coordination polymers and metal-organic frameworks due to its ability to form stable coordination complexes with metal ions. This application is crucial for creating materials with tailored properties for various applications, such as gas storage, catalysis, and sensing.
Used in Catalysis:
2,4,6-tris(4-formylphenyl)pyridine is used as a catalyst or catalyst precursor in various chemical reactions. Its formyl groups can act as active sites for catalytic processes, enabling the compound to facilitate transformations in organic synthesis, such as oxidation, reduction, and coupling reactions.
Used in Luminescence:
2,4,6-tris(4-formylphenyl)pyridine is used in the development of luminescent materials due to its ability to emit light upon excitation. This property makes it suitable for applications in optoelectronics, such as organic light-emitting diodes (OLEDs) and sensors for detecting specific analytes.
Used in Material Science:
2,4,6-tris(4-formylphenyl)pyridine is used in the design and synthesis of novel materials with unique properties, such as high thermal stability, mechanical strength, and electrical conductivity. These materials can be employed in various industries, including aerospace, automotive, and electronics.
Used in Biological Activities Research:
2,4,6-tris(4-formylphenyl)pyridine has been studied for its potential biological activities, such as antimicrobial, antiviral, and anticancer properties. Its ability to interact with biological targets makes it a promising candidate for the development of new therapeutic agents and diagnostic tools in the field of medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 2230887-26-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,2,3,0,8,8 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2230887-26:
(9*2)+(8*2)+(7*3)+(6*0)+(5*8)+(4*8)+(3*7)+(2*2)+(1*6)=158
158 % 10 = 8
So 2230887-26-8 is a valid CAS Registry Number.
2230887-26-8Relevant articles and documents
Strategic design of triphenylamine- and triphenyltriazine-based two-dimensional covalent organic frameworks for CO2 uptake and energy storage
El-Mahdy, Ahmed F. M.,Kuo, Cheng-Han,Alshehri, Abdulmohsen,Young, Christine,Yamauchi, Yusuke,Kim, Jeonghun,Kuo, Shiao-Wei
, p. 19532 - 19541 (2018)
Hexagonally ordered covalent organic frameworks (COFs) are interesting new crystalline porous materials that have massive potential for application in gas storage. Herein, we report the synthesis of two series of two-dimensional hexagonally ordered COFs - TPA-COFs and TPT-COFs - through one-pot polycondensations of tris(4-aminophenyl)amine (TPA-3NH2) and 2,4,6-tris(4-aminophenyl)triazine (TPT-3NH2), respectively, with triarylaldehydes featuring different degrees of planarity, symmetry, and nitrogen content. All the synthesized COFs exhibited high crystallinity, large BET surface areas (up to 1747 m2 g-1), excellent thermal stability, and pore size distributions from 1.80 to 2.55 nm. The symmetry and planarity of the monomers strongly affected the degrees of crystallinity and the BET surface areas of the resultant COFs. In addition, these COFs displayed excellent CO2 uptake efficiencies of up to 65.65 and 92.38 mg g-1 at 298 and 273 K, respectively. The incorporation of the more planar and higher-nitrogen-content triaryltriazine unit into the backbones of the TPA-COFs and TPT-COFs enhanced the interactions with CO2, leading to higher CO2 uptakes. Moreover, the synthesized COFs exhibited electrochemical properties because of their conjugated structures containing redox-active triphenylamine groups. This study exposes the importance of considering the symmetry and planarity of the monomers when designing highly crystalline COFs; indeed, the structures of COFs can be tailored to vary their functionalities for specific applications.
