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Product Line: Pharmaceutical Chemicals

2,5-dichloropyridine-3-carbaldehyde

CAS 176433-49-1

Molecular structure of 2,5-dichloropyridine-3-carbaldehyde

CAS · 176433-49-1

01

Product Overview

2,5-dichloropyridine-3-carbaldehyde 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 solid
Purity (HPLC): 98% min
Water (KF): 0.5% max
H NMR: Correct structure
03

Applications

2,5-Dichloropyridine-3-carbaldehyde is a halogenated pyridine aldehyde widely used as an intermediate in pharmaceutical and agrochemical synthesis. Its aldehyde group and dichloro-substituted pyridine ring provide reactive sites for condensation, nucleophilic addition, and cross-coupling reactions. It is commonly employed in the synthesis of heterocyclic compounds, kinase inhibitors, antiviral and anticancer drug candidates, and other bioactive molecules. Additionally, it is used in chemical research for developing novel functionalized pyridine derivatives, ligands, and specialty fine chemicals. Its versatility makes it valuable in both medicinal chemistry and materials science applications.

04

Benefits

The compound offers high chemical reactivity due to the combination of electron-withdrawing chloro groups and an aldehyde functional group, allowing selective transformations and efficient multistep syntheses. Its pyridine ring provides chemical stability while enabling derivatization to form diverse heterocyclic scaffolds. It is soluble in common organic solvents and compatible with a variety of reaction conditions, ensuring reproducibility and high yields. These properties make it a reliable and efficient intermediate for the preparation of complex molecules in pharmaceutical and chemical research.

05

Conclusion

2,5-Dichloropyridine-3-carbaldehyde is a versatile and reactive intermediate used in pharmaceuticals, agrochemicals, and fine chemical synthesis. Its dual chloro substituents and aldehyde functionality support selective chemical transformations, enabling the efficient production of heterocyclic compounds, bioactive molecules, and advanced chemical intermediates.

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