2-Fluoro-5-bromopyridine CAS#766-11-0
2-Fluoro-5-bromopyridine , Promotion Season Now in Store and Free Sample for Testing with Factory Price
Chemical Name: 2-Fluoro-5-bromopyridine
CAS No.: 766-11-0
Molecular Formula: C5H3BrFN
Molecular weight: 175.99
Sample: Available

2-Fluoro-5-bromopyridine: The Complete Guide
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Basic Info of 2-Fluoro-5-bromopyridine
Chemical Name | 2-Fluoro-5-bromopyridine |
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Synonyms | Halogenated;Organohalides; Bromopyridines;Fluoropyridines; Halopyridines;BoronicAcid; C5HeterocyclicBuildingBlocks; HalogenatedHeterocycles; HeterocyclicBuildingBlocks;Pyridine;pharmacetical; Pyridinesderivates;PyridineSeries;Fluorineseries |
CAS No. | 766-11-0 |
Molecular Formula | C5H3BrFN |
Molecular Weight | 175.99 |
Safety Info
HS Code | 29339900 |
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WGK Germany | 3 |
Properties
Appearance & Physical State | Clear colorless yellow |
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Density | 1.71 g/mL at 25 °C(lit.) |
Boiling Point | 162-164 °C750 mm Hg(lit.) |
Melting Point | 165 °F |
Flash Point | 104.8ºC |
Refractive Index | 1.710 |
Numbering system
UNIT | TD34B3O8M9 |
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What is 2-Fluoro-5-bromopyridine?
With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is 2-Fluoro-5-bromopyridine which has developed particularly rapidly in recent years. Do you know about 2-Fluoro-5-bromopyridine?
The official answer: 5-Bromo-2-fluoropyridine, 5-Bromo-2-fluoropyridine, molecular formula C5H3BrFN.
What’s the application of 2-Fluoro-5-bromopyridine?
2-Fluoro-5-bromopyridine is used in the synthesis of heteroaromatic and aniline derivatives of piperidine as an effective ligand for acetylcholine vesicular transport. It is also used in the synthesis of benzofurano[3,2-d]pyrimidine-2-one derivatives. Uses 2-fluoro-5-bromopyridine is an organic synthesis intermediate and pharmaceutical intermediate, which can be used in laboratory research and development process and chemical and pharmaceutical synthesis process.
Conclusion
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