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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2-Bromo-5-chloro-3-fluoropyridine

AB43854

514797-97-8 | 2-Bromo-5-chloro-3-fluoropyridine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $15.00 $10.00 -   +
1g 97% in stock $15.00 $11.00 -   +
5g 97% in stock $20.00 $14.00 -   +
25g 97% in stock $60.00 $42.00 -   +
100g 97% in stock $204.00 $143.00 -   +
500g 97% in stock $952.00 $667.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB43854
Chemical Name: 2-Bromo-5-chloro-3-fluoropyridine
CAS Number: 514797-97-8
Molecular Formula: C5H2BrClFN
Molecular Weight: 210.4315
MDL Number: MFCD11044268
SMILES: Clc1cnc(c(c1)F)Br

 

Computed Properties
Complexity: 103  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
XLogP3: 2.6  

 

 

Upstream Synthesis Route
  • 2-Bromo-5-chloro-3-fluoropyridine is a versatile chemical compound commonly used in organic synthesis. Its unique molecular structure makes it a valuable building block in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. This compound serves as a key intermediate in the synthesis of complex molecules due to its reactivity and ability to undergo various chemical transformations.In chemical synthesis, 2-Bromo-5-chloro-3-fluoropyridine is often employed as a halogenated heterocycle, enabling the introduction of functional groups and facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Its presence in a molecular scaffold can significantly influence the properties and activities of the final product. Additionally, this compound's selective halogenation pattern allows for precise modifications during multi-step synthesis processes.Moreover, the strategic placement of bromine, chlorine, and fluorine atoms in 2-Bromo-5-chloro-3-fluoropyridine grants it a high level of synthetic utility, making it an essential reagent in the development of new chemical entities with potential therapeutic or agricultural applications. Its versatility and compatibility with various reaction conditions make it a valuable tool for chemists seeking to design and produce novel compounds with enhanced biological activities or improved properties.
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