2-(1,1-biphenyl-3-yl)-4-chloro-6-phenyl-1,3,5-triazine丨CAS 1689576-03-1

2-(1,1-biphenyl-3-yl)-4-chloro-6-phenyl-1,3,5-triazine丨CAS 1689576-03-1
Product Introduction:
Catalog No.: SS083488
CAS No.: 1689576-03-1
Purity: 98%min
Product Name: 2-(1,1-biphenyl-3-yl)-4-chloro-6-phenyl-1,3,5-triazine
Molecular Formula: C21H14ClN3
Molecular Weight: 343.81
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 2-(1,1-biphenyl-3-yl)-4-chloro-6-phenyl-1,3,5-triazine丨cas 1689576-03-1 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance Off white powder
Purity 98% min.

 

 

 

Applications

 

2-(1,1-biphenyl-3-yl)-4-chloro-6-phenyl-1,3,5-triazine is primarily used in the field of advanced materials and organic electronics. Its rigid triazine core, combined with biphenyl and phenyl substituents, provides excellent thermal and photochemical stability, making it suitable as a building block in organic semiconductors, light-emitting diodes (OLEDs), and photovoltaic devices. The compound's chloro functionality allows it to undergo further chemical modification, enabling the synthesis of polymers, small molecules, and dendrimers with tailored electronic properties. It is also applied in the design of fluorescent probes, optoelectronic materials, and as an intermediate in the production of high-performance resins and coatings. Its combination of stability, planarity, and conjugated structure makes it a versatile component in both research and industrial-scale development of functional materials.

 

Benefits

 

The benefits of this compound stem from its structural rigidity, electronic tunability, and chemical reactivity. Its triazine core contributes to thermal stability and resistance to oxidative degradation, which is critical in high-performance electronic and photonic applications. The biphenyl and phenyl substituents enhance π-conjugation, improving charge transport and light-emitting efficiency when used in optoelectronic devices. The chloro group allows selective substitution reactions, giving chemists flexibility to design derivatives with precise electronic and physical properties. This versatility supports innovations in materials science, including the development of efficient OLED emitters, stable organic semiconductors, and functional polymers with high thermal and mechanical robustness. Additionally, its predictable reactivity and compatibility with a wide range of synthetic protocols make it an efficient intermediate in complex molecular architectures, supporting cost-effective and reproducible production processes.

 

Conclusion

 

In summary, 2-(1,1-biphenyl-3-yl)-4-chloro-6-phenyl-1,3,5-triazine is a highly valuable compound for advanced materials and organic electronics. Its combination of thermal stability, electronic conjugation, and chemical modifiability allows it to serve as both a functional building block and a versatile intermediate in synthesis. The compound's benefits-ranging from improved device performance to flexible chemical derivatization-make it indispensable in the development of high-performance optoelectronic materials and innovative polymer systems. Its continued use facilitates progress in electronics, photonics, and materials chemistry, supporting both industrial and research applications.

 

 

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