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Product Line: Pharmaceutical Chemicals

2-Chloro-3-fluoropyridine

CAS 17282-04-1

Molecular structure of 2-Chloro-3-fluoropyridine

CAS · 17282-04-1

01

Product Overview

2-Chloro-3-fluoropyridine is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance Colorless to light yellow liquid
Purity (GC) 98% min
Water content 0.5% max
03

Applications

2-Chloro-3-fluoropyridine is a valuable halogenated pyridine derivative widely applied as an intermediate in pharmaceutical, agrochemical, and fine chemical synthesis. It is commonly used in the preparation of active pharmaceutical ingredients (APIs), serving as a building block for drugs targeting inflammation, cancer, and infectious diseases. In agrochemicals, it contributes to the development of herbicides, fungicides, and insecticides due to its heteroaryl scaffold and reactivity. It is also employed in materials chemistry, where its halogen functionalities enable cross-coupling reactions such as Suzuki or Buchwald-Hartwig reactions, facilitating the creation of advanced heterocyclic compounds.

04

Benefits

The benefits of 2-Chloro-3-fluoropyridine stem from its dual halogen substitution, which enhances reactivity and selectivity in synthetic transformations. The chlorine and fluorine atoms provide versatile functional handles for substitution and coupling reactions, enabling efficient derivatization. Its pyridine core imparts stability and desirable electronic properties, making it a reliable intermediate for synthesizing bioactive molecules. Additionally, its compatibility with modern synthetic methods, such as palladium-catalyzed coupling, makes it a cost-effective and scalable choice for industrial applications.

05

Conclusion

2-Chloro-3-fluoropyridine is a versatile chemical intermediate that supports innovation in pharmaceuticals, agrochemicals, and advanced material synthesis. Its benefits include enhanced reactivity, selectivity, and adaptability in coupling reactions, ensuring its ongoing importance in the development of high-value chemical products.

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