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Specifications of 2-chloro-4-(4-(naphthalen-1-yl)phenyl)-6-phenyl-1,3,5-triazine丨CAS 2229752-36-5
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Appearance |
Off-white or white powder |
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Purity |
99% min |
Applications of 2-chloro-4-(4-(naphthalen-1-yl)phenyl)-6-phenyl-1,3,5-triazine丨CAS 2229752-36-5
1. Organic Electronics and Optoelectronics
Utilized as a building block or functional material in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and other optoelectronic devices due to its aromatic and heterocyclic structure.
The triazine core offers good electron-accepting properties, making it valuable in electron transport layers and as a host material in OLEDs.
2. Pharmaceutical and Agrochemical Intermediate
Serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals where the triazine scaffold is present.
Useful for the design and development of compounds with potential biological activities.
3. Material Science
Incorporated into polymeric materials and coatings to enhance thermal stability, rigidity, and chemical resistance.
Can be used in crosslinking agents and specialty resins due to its reactive chlorine atom on the triazine ring.
4. Chemical Research
Employed in organic synthesis and materials chemistry for the development of novel functional molecules.
Useful for studies involving substitution reactions on the triazine ring.
Benefits
✅ Strong Electron-Accepting Properties
The triazine ring provides efficient electron-withdrawing capabilities, important for electronic and photonic applications.
✅ Structural Versatility
The combination of aromatic groups (naphthyl and phenyl) with the triazine core offers rigidity and conjugation, beneficial for material stability and optical properties.
✅ Reactive Site for Functionalization
The chlorine substituent allows for further chemical modifications, enabling tailored molecule design.
Summary
2-chloro-4-(4-(naphthalen-1-yl)phenyl)-6-phenyl-1,3,5-triazine丨CAS 2229752-36-5 is a versatile triazine derivative widely used in organic electronics, pharmaceuticals, and materials science. Its electron-accepting triazine core combined with aromatic substituents makes it valuable in OLEDs, optoelectronic devices, and as a synthetic intermediate. The reactive chlorine atom enables further functionalization for customized applications.
