3-Fluoro-2-pyridinecarboxaldehyde丨CAS 31224-43-8

3-Fluoro-2-pyridinecarboxaldehyde丨CAS 31224-43-8
Product Introduction:
Catalog No.: SS056798
CAS No.: 31224-43-8
Purity(GC): 98%min
Product Name: 3-Fluoro-2-pyridinecarboxaldehyde
Molecular Formula: C6H4FNO
Molecular Weight: 125.1
Synonym(s): 3-fluoro-2-formylpyridine
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Technical Parameters
Description

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Specifications of 3-Fluoro-2-pyridinecarboxaldehyde丨CAS 31224-43-8

 

Appearance:

Off white to light yellow solid

Purity (GC):

98%min

Water (KF):

0.5%max

 

 

 

Applications

1. Pharmaceutical Intermediate

3-Fluoro-2-pyridinecarboxaldehyde丨CAS 31224-43-8 is widely used as a key building block in the synthesis of pharmaceutical compounds:

Drug Discovery and Development:
The aldehyde group allows for the creation of imines, oximes, and other derivatives that are critical in medicinal chemistry.
The fluorine atom can improve bioavailability, metabolic stability, and target binding of drug candidates.

Heterocyclic Compound Synthesis:
It serves as a precursor for more complex heterocyclic scaffolds, especially in anti-inflammatory, antiviral, and oncology-related drug research.

Fragment-Based Drug Design (FBDD):
Its small molecular size and functional diversity make it suitable for use in fragment libraries for high-throughput screening.


2. Agrochemical Intermediate

Synthesis of Crop Protection Agents:
Fluorinated pyridine derivatives are important in the development of herbicides, fungicides, and insecticides due to their metabolic resistance and selective bioactivity.

Enhancement of Efficacy and Selectivity:
Fluorine substitution often enhances lipophilicity, membrane permeability, and target affinity in agrochemical molecules.


3. Organic Synthesis and Specialty Chemicals

Ligand and Catalyst Design:
The pyridine ring can act as a chelating ligand in organometallic and coordination chemistry.
The aldehyde group allows further functionalization to synthesize customized ligands.

Synthesis of Fluorinated Materials:
Fluorinated aromatic aldehydes are precursors for specialty polymers and liquid crystals, especially where precise molecular orientation and thermal stability are needed.


4. Research and Development

Synthetic Route Optimization:
Used as a model substrate in developing selective reactions involving fluorinated aromatics or aldehyde chemistry.

Fluorine Chemistry Studies:
Helps explore the electronic effects of fluorine in heteroaromatic systems, often used in academic and industrial R&D.


 

Benefits

1. Dual Functional Reactivity

The aldehyde group is highly reactive, suitable for condensation, cyclization, and cross-coupling reactions.

The fluorine atom influences electronic distribution, improving reactivity control and enabling regioselective transformations.

2. Bioactive Potential

Fluorine enhances pharmacokinetic properties such as metabolic resistance and cell permeability.

The pyridine ring is a privileged structure in medicinal chemistry, often found in FDA-approved drugs.

3. Versatility in Derivatization

Can be converted into:

Amines (via reductive amination)

Alcohols (via reduction)

Heterocycles (via condensation or cycloaddition)

Oximes, hydrazones, and Schiff bases

This versatility makes it a valuable intermediate in both small-scale research and large-scale synthesis.


 

Conclusion

3-Fluoro-2-pyridinecarboxaldehyde丨CAS 31224-43-8 is a highly useful fluorinated aromatic aldehyde with applications spanning pharmaceutical development, agrochemical synthesis, specialty chemical production, and academic research. Its unique combination of reactivity and fluorine-enhanced properties makes it a go-to intermediate for synthesizing bioactive molecules, advanced materials, and functionalized heterocycles.

 

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