2,6-Dichloronicotinic Acid丨CAS 38496-18-3

2,6-Dichloronicotinic Acid丨CAS 38496-18-3
Product Introduction:
Catalog No.: SS122952
CAS No.: 38496-18-3
Purity(HPLC): 95% min
Product Name: 2,6-Dichloronicotinic acid
Molecular Formula: C6H3Cl2NO2
Molecular Weight: 192
Synonym(s): 2,6-Dichloropyridine-3-carboxylic acid
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Technical Parameters
Description

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Specifications

 

Item Specification
Appearance White to yellow solid
Water (KF) 0.5% max
Single impurity (HPLC) 1.0% max
Purity (HPLC) 95% min

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2933399099306

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed in a dry and well-ventilated place.

Condition to Avoid

 

Package

 

 

Manufacturing Information

 

Parameter

Specification

Capacity

10MT/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2015

Stock

 

 

 

 

Applications

 

2,6-Dichloronicotinic acid (CAS 38496-18-3) is a halogenated pyridinecarboxylic acid widely used as an intermediate in pharmaceuticals, agrochemicals, and fine chemical synthesis. Its dichloro-substituted pyridine ring, combined with the carboxylic acid functionality, makes it a versatile scaffold for building heterocyclic compounds, enzyme inhibitors, and receptor ligands. In medicinal chemistry, it is employed in the synthesis of drug candidates where halogenation improves metabolic stability and binding affinity. In agrochemicals, it serves as a precursor for herbicides, fungicides, and insecticides with enhanced potency and environmental resilience. It is also applied in material science and coordination chemistry, where its pyridine and carboxyl groups provide useful sites for metal-ligand interactions.

 

Benefits

 

The benefits of 2,6-dichloronicotinic acid lie in its dual reactivity and functional versatility. The chloro substituents are excellent leaving groups, enabling cross-coupling and substitution reactions to introduce diverse functional groups. The carboxylic acid group allows transformations such as esterification, amidation, or salt formation, expanding its synthetic utility. The pyridine ring contributes rigidity and electronic effects, enhancing biological activity and stability in derived compounds. These combined features make it a highly adaptable building block for efficient multi-step syntheses across pharmaceutical, agrochemical, and material chemistry applications.

 

Conclusion

 

In summary, 2,6-dichloronicotinic acid is a valuable intermediate with broad applications in pharmaceuticals, agrochemicals, and materials science. Its applications include drug precursor synthesis, crop-protection agent development, and coordination compound preparation, while its benefits come from reactive chloro substituents, versatile carboxyl chemistry, and biologically relevant pyridine scaffolding. As demand for halogenated heterocycles continues to rise, this compound remains an important tool in modern synthetic chemistry.

 

 

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