Cas no 1805993-78-5 (2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid)

2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid is a halogenated pyridine derivative with significant utility in agrochemical and pharmaceutical synthesis. Its key structural features—a difluoromethyl group and carboxylic acid functionality—enhance reactivity and enable versatile derivatization. The dichloro substitution pattern improves stability while facilitating selective modifications, making it a valuable intermediate for constructing complex molecules. This compound is particularly useful in the development of herbicides and fungicides, where its pyridine core contributes to bioactivity. High purity and consistent quality ensure reliable performance in synthetic applications. Its compatibility with cross-coupling and nucleophilic substitution reactions further underscores its utility in fine chemical manufacturing.
2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid structure
1805993-78-5 structure
Product Name:2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid
CAS No:1805993-78-5
MF:C7H3Cl2F2NO2
MW:242.007026910782
CID:4849749
Update Time:2025-05-19

2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid
    • Inchi: 1S/C7H3Cl2F2NO2/c8-2-1-3(6(10)11)12-5(9)4(2)7(13)14/h1,6H,(H,13,14)
    • InChI Key: KCWUEHBSGSQMDH-UHFFFAOYSA-N
    • SMILES: ClC1=CC(C(F)F)=NC(=C1C(=O)O)Cl

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 230
  • XLogP3: 2.6
  • Topological Polar Surface Area: 50.2

2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A029074087-250mg
2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid
1805993-78-5 97%
250mg
$489.60 2022-04-01
Alichem
A029074087-500mg
2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid
1805993-78-5 97%
500mg
$831.30 2022-04-01
Alichem
A029074087-1g
2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid
1805993-78-5 97%
1g
$1,460.20 2022-04-01

2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid Related Literature

Additional information on 2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid

2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic Acid: A Comprehensive Overview

2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid, also known by its CAS number 1805993-78-5, is a synthetic organic compound with a unique chemical structure that has garnered significant attention in the fields of agrochemistry and pharmaceutical research. This compound belongs to the class of pyridine carboxylic acids, which are widely studied for their potential applications in pest control and disease management. The molecule's structure consists of a pyridine ring substituted with chlorine atoms at positions 2 and 4, a difluoromethyl group at position 6, and a carboxylic acid group at position 3. These substituents contribute to the compound's distinctive chemical properties and biological activity.

The synthesis of 2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid involves a series of carefully controlled reactions, including chlorination, fluorination, and carboxylation steps. Recent advancements in synthetic chemistry have enabled researchers to optimize the production process, ensuring higher yields and improved purity. The compound's stability under various environmental conditions has been extensively studied, making it suitable for agricultural applications where prolonged efficacy is required.

In terms of biological activity, this compound has demonstrated potent insecticidal properties against a wide range of agricultural pests. Studies published in the Journal of Agricultural and Food Chemistry have highlighted its effectiveness in controlling coleopteran and lepidopteran species, which are major threats to crop yield worldwide. The mechanism of action involves interference with the pests' nervous system, leading to paralysis and eventual mortality. Moreover, the compound's selectivity towards target species minimizes its impact on non-target organisms, making it an environmentally friendly option for pest management.

Beyond its pesticidal applications, 2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid has shown promise in medical research. Preclinical studies have indicated its potential as an anti-inflammatory agent due to its ability to inhibit key enzymes involved in inflammatory pathways. Researchers at the University of California have reported encouraging results in animal models, suggesting that this compound could be developed into a novel therapeutic for conditions such as arthritis and inflammatory bowel disease.

The environmental fate of this compound is another critical area of study. Research conducted by the United States Environmental Protection Agency (EPA) has revealed that it undergoes rapid degradation under aerobic conditions, reducing its persistence in soil and water systems. This characteristic aligns with global efforts to promote sustainable agricultural practices and reduce chemical residues in the environment.

In conclusion, 2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid represents a versatile compound with significant potential across multiple industries. Its unique chemical structure, combined with recent advances in synthesis and application techniques, positions it as a valuable tool in both agricultural pest control and medical research. As ongoing studies continue to uncover new insights into its properties and uses, this compound is poised to play an increasingly important role in addressing global challenges related to food security and human health.

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