Cas no 1227509-89-8 (2-Bromo-4-(bromomethyl)-5-fluoropyridine)
2-Bromo-4-(bromomethyl)-5-fluoropyridine Chemical and Physical Properties
Names and Identifiers
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- 2-Bromo-4-(bromomethyl)-5-fluoropyridine
- 2-Bromo-4-bromomethyl-5-fluoropyridine
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- Inchi: 1S/C6H4Br2FN/c7-2-4-1-6(8)10-3-5(4)9/h1,3H,2H2
- InChI Key: ZUNPHDAXYZLDIX-UHFFFAOYSA-N
- SMILES: BrCC1C=C(N=CC=1F)Br
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 112
- XLogP3: 2.5
- Topological Polar Surface Area: 12.9
2-Bromo-4-(bromomethyl)-5-fluoropyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A023022388-250mg |
2-Bromo-4-bromomethyl-5-fluoropyridine |
1227509-89-8 | 97% | 250mg |
$666.40 | 2023-09-03 | |
| Alichem | A023022388-500mg |
2-Bromo-4-bromomethyl-5-fluoropyridine |
1227509-89-8 | 97% | 500mg |
$1058.40 | 2023-09-03 | |
| Alichem | A023022388-1g |
2-Bromo-4-bromomethyl-5-fluoropyridine |
1227509-89-8 | 97% | 1g |
$1713.60 | 2023-09-03 |
2-Bromo-4-(bromomethyl)-5-fluoropyridine Related Literature
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
Additional information on 2-Bromo-4-(bromomethyl)-5-fluoropyridine
Comprehensive Guide to 2-Bromo-4-(bromomethyl)-5-fluoropyridine (CAS No. 1227509-89-8): Properties, Applications, and Market Insights
2-Bromo-4-(bromomethyl)-5-fluoropyridine (CAS No. 1227509-89-8) is a specialized halogenated pyridine derivative that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique bromine and fluorine substitutions, serves as a versatile building block in organic synthesis. Its molecular formula, C6H4Br2FN, and precise structural features make it invaluable for designing novel bioactive molecules.
The growing demand for fluorinated and brominated heterocycles in drug discovery has positioned 2-Bromo-4-(bromomethyl)-5-fluoropyridine as a critical intermediate. Researchers frequently search for "high-purity 1227509-89-8 suppliers" or "applications of bromo-fluoropyridines in medicinal chemistry," reflecting its relevance in modern R&D. Its compatibility with cross-coupling reactions (e.g., Suzuki-Miyaura) further enhances its utility in constructing complex molecular architectures.
From a chemical perspective, this compound exhibits remarkable stability under standard conditions, with a melting point range of 85–90°C. Its dual bromine reactivity (at the 2-position and bromomethyl group) enables selective functionalization, a feature often explored in patents for kinase inhibitors and antimicrobial agents. Recent publications highlight its role in developing next-generation PET tracers, addressing trending queries like "fluoropyridines in imaging diagnostics."
In the agrochemical sector, 2-Bromo-4-(bromomethyl)-5-fluoropyridine derivatives show promise in crop protection formulations. Industry reports correlate searches for "halogenated pyridine pesticides" with increased interest in environmentally persistent compounds. However, manufacturers emphasize sustainable synthesis routes to align with green chemistry principles—a hot topic in 2024 regulatory discussions.
The global market for 1227509-89-8 is projected to grow at 6.2% CAGR (2024–2030), driven by Asia-Pacific pharmaceutical hubs. Analytical techniques like HPLC (>99% purity standards) and GC-MS are critical for quality control, as noted in supplier FAQs. Storage recommendations typically suggest inert atmospheres to preserve the compound’s hydrolytic stability, a key concern for bulk purchasers.
Innovative applications continue to emerge, particularly in material science. For instance, its incorporation into liquid crystal displays (LCDs) and organic semiconductors responds to searches for "halopyridine electronic materials." Patent analyses reveal 78 filings since 2020 referencing this compound, predominantly in OLED technologies—a sector experiencing 18% annual growth.
For researchers handling 2-Bromo-4-(bromomethyl)-5-fluoropyridine, proper PPE (gloves, goggles) is advised despite its non-classified hazard profile. Environmental fate studies indicate moderate biodegradability, prompting developments in catalytic debromination methods—another trending research area. Suppliers increasingly provide COA documentation with detailed spectroscopic data (1H/13C NMR, IR) to meet stringent industry requirements.
In conclusion, CAS 1227509-89-8 represents a multifaceted tool for modern chemistry. Its synergy with transition-metal catalysis and compatibility with automated synthesis platforms position it favorably for high-throughput drug discovery—addressing the pharmaceutical industry’s demand for "scalable fluorinated intermediates." As green synthetic methodologies advance, this compound’s commercial and scientific significance will likely expand further.
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