Cas no 1805993-78-5 (2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid)
2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid Chemical and Physical Properties
Names and Identifiers
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- 2,4-Dichloro-6-(difluoromethyl)pyridine-3-carboxylic acid
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- 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
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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2. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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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