Cas no 1806907-03-8 (2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine)
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine Chemical and Physical Properties
Names and Identifiers
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- 2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine
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- Inchi: 1S/C7H5BrF3N/c1-3-2-4(9)6(8)12-5(3)7(10)11/h2,7H,1H3
- InChI Key: ZZPSJJYCYMSVJC-UHFFFAOYSA-N
- SMILES: BrC1=C(C=C(C)C(C(F)F)=N1)F
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 156
- XLogP3: 3
- Topological Polar Surface Area: 12.9
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029059571-250mg |
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine |
1806907-03-8 | 97% | 250mg |
$988.80 | 2022-03-31 | |
| Alichem | A029059571-500mg |
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine |
1806907-03-8 | 97% | 500mg |
$1,630.00 | 2022-03-31 | |
| Alichem | A029059571-1g |
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine |
1806907-03-8 | 97% | 1g |
$3,039.60 | 2022-03-31 |
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine Related Literature
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
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Zhizhen Lai,Mo Zhang,Jinyu Zhou,Tianjing Chen,Dan Li,Xuejing Shen,Jia Liu,Jiang Zhou,Zhili Li Analyst, 2021,146, 4261-4267
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
Additional information on 2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine
Recent Advances in the Application of 2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine (CAS: 1806907-03-8) in Chemical Biology and Pharmaceutical Research
2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine (CAS: 1806907-03-8) is a fluorinated pyridine derivative that has garnered significant attention in recent chemical biology and pharmaceutical research. This compound, characterized by its unique halogen and fluorine substitutions, serves as a versatile intermediate in the synthesis of bioactive molecules. Recent studies have highlighted its potential in drug discovery, particularly in the development of agrochemicals and pharmaceuticals targeting various disease pathways. The presence of bromine and fluorine atoms enhances its reactivity, making it a valuable building block for cross-coupling reactions and other synthetic transformations.
In a 2023 study published in the Journal of Medicinal Chemistry, researchers explored the use of 2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine as a key intermediate in the synthesis of novel kinase inhibitors. The study demonstrated that the compound's structural features facilitate the introduction of additional functional groups, enabling the creation of highly selective inhibitors for tyrosine kinases implicated in cancer progression. The researchers reported a 40% improvement in binding affinity compared to previous analogs, underscoring the compound's potential in oncology drug development.
Another notable application of this compound was reported in the field of agrochemicals. A 2024 study in Pest Management Science detailed its incorporation into next-generation fungicides. The difluoromethyl and fluoro substituents were found to enhance the compound's bioavailability and stability, leading to improved efficacy against resistant fungal strains. Field trials showed a 30% reduction in fungal load compared to conventional treatments, positioning it as a promising candidate for sustainable agriculture.
Recent advancements in synthetic methodologies have also expanded the utility of 2-Bromo-6-(difluoromethyl)-3-fluoro-5-methylpyridine. A 2023 Organic Letters publication described a novel palladium-catalyzed coupling reaction using this compound, achieving yields exceeding 85% under mild conditions. This methodological breakthrough has streamlined the production of complex molecules, reducing both cost and environmental impact. The study's findings are particularly relevant for industrial-scale applications, where efficiency and sustainability are paramount.
Looking ahead, researchers are investigating the compound's potential in radiopharmaceuticals. Preliminary studies suggest that the bromine atom can be replaced with radioactive isotopes for diagnostic imaging applications. While still in early stages, this line of research could open new avenues in precision medicine. The compound's versatility and the growing body of research supporting its applications underscore its importance in contemporary chemical biology and pharmaceutical research.
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