Cas no 1804858-95-4 (6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride)
6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride Chemical and Physical Properties
Names and Identifiers
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- 6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride
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- Inchi: 1S/C7H5Cl2F2NO2S/c1-3-6(15(9,13)14)4(7(10)11)2-5(8)12-3/h2,7H,1H3
- InChI Key: UNYXMFSLGHDSNJ-UHFFFAOYSA-N
- SMILES: ClS(C1C(C)=NC(=CC=1C(F)F)Cl)(=O)=O
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
- Complexity: 319
- XLogP3: 2.9
- Topological Polar Surface Area: 55.4
6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029045904-1g |
6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride |
1804858-95-4 | 97% | 1g |
$1,564.50 | 2022-04-01 |
6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride Related Literature
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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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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
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Daniel Messmer,Stefan Salentinig,Jakob Heier Nanoscale, 2019,11, 6929-6938
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
Additional information on 6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride
6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride (CAS No. 1804858-95-4)
The compound 6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride (CAS No. 1804858-95-4) is a highly specialized organic chemical with significant applications in various industries. This compound belongs to the class of pyridine sulfonyl chlorides, which are widely used as intermediates in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The structure of this compound is characterized by a pyridine ring substituted with chlorine, a difluoromethyl group, and a methyl group at specific positions, along with a sulfonyl chloride functional group.
Recent studies have highlighted the importance of pyridine sulfonyl chlorides in the development of novel bioactive molecules. The sulfonyl chloride group is particularly valuable due to its reactivity in nucleophilic substitution reactions, making it an ideal building block for constructing complex molecular architectures. The presence of chlorine and difluoromethyl substituents further enhances the compound's versatility, enabling it to participate in a wide range of chemical transformations.
The synthesis of 6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride involves a multi-step process that typically begins with the preparation of the corresponding pyridine derivative. Advanced methodologies, such as microwave-assisted synthesis and catalytic processes, have been employed to optimize the production efficiency and minimize environmental impact. These techniques not only improve yield but also ensure the purity required for high-performance applications.
In terms of applications, this compound has garnered significant attention in the field of agricultural chemistry. It serves as a key intermediate in the synthesis of pesticides and herbicides, where its ability to target specific biochemical pathways makes it highly effective. Recent research has demonstrated its potential as a component in next-generation crop protection agents, offering improved efficacy while reducing environmental toxicity.
Beyond agriculture, 6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride is also explored in the pharmaceutical industry for its role in drug discovery. Its unique structure allows for the creation of bioisosteres and prodrugs, which are critical in developing drugs with enhanced pharmacokinetic profiles. Collaborative efforts between academic institutions and pharmaceutical companies have led to breakthroughs in leveraging this compound for therapeutic applications.
The environmental impact and safety profile of this compound are subjects of ongoing research. Studies focus on its degradation pathways under various conditions and its potential effects on non-target organisms. Regulatory bodies require stringent testing to ensure compliance with safety standards, which underscores the importance of thorough toxicological evaluations.
In conclusion, 6-Chloro-4-(difluoromethyl)-2-methylpyridine-3-sulfonyl chloride (CAS No. 1804858-95-4) stands as a pivotal molecule in modern chemistry. Its versatility, reactivity, and applicability across multiple domains position it as a valuable asset in both industrial and academic settings. As research continues to uncover new potentials, this compound is expected to play an even more prominent role in driving innovation across various sectors.
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