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Product Line: Pharmaceutical Chemicals

2-Chloro-5-fluoropyridin-3-amine

CAS 884495-37-8

Molecular structure of 2-Chloro-5-fluoropyridin-3-amine

CAS · 884495-37-8

01

Product Overview

2-Chloro-5-fluoropyridin-3-amine 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: White to light yellow powder
Purity: 98% min
Water: 0.5% max
03

Applications

 

 

1. Pharmaceutical Intermediate

Used in the synthesis of active pharmaceutical ingredients (APIs), particularly in the development of kinase inhibitors, antivirals, or anti-inflammatory drugs.

The halogenated pyridine scaffold is prevalent in medicinal chemistry due to its metabolic stability and bioactivity potential.

2. Agrochemical Synthesis

Acts as a building block in the development of herbicides, fungicides, and pesticides.

Fluoro- and chloro-substituents improve lipophilicity and biological potency.

3. Cross-Coupling Reactions

The chlorine atom can undergo Suzuki, Buchwald-Hartwig, or Stille coupling reactions for further substitution.

The amine group enables amide bond formation and heterocyclic ring construction.

04

Benefits

 

✅ Versatile Functional Groups

The combination of –NH₂, –Cl, and –F provides multiple reactive handles for chemical synthesis.

✅ High Reactivity

Facilitates coupling reactions and derivatization for complex molecule construction.

✅ Useful Scaffold

Pyridine ring systems are core components in a wide range of bioactive compounds.

✅ Electron-Withdrawing Effects

Halogens modulate the electronic nature of the molecule, useful for tuning activity in drug and agrochemical design.

05

Conclusion

2-Chloro-5-fluoropyridin-3-amine (CAS 884495-37-8) is a highly valuable intermediate in medicinal and agrochemical chemistry, offering multifunctional reactivity due to its halogenated pyridine backbone and amine group. Its role in complex synthesis makes it a go-to choice for building biologically active molecules.

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