logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 3-Bromo-6-chloro-2-fluoropyridine

AB64516

885952-18-1 | 3-Bromo-6-chloro-2-fluoropyridine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $7.00 $5.00 -   +
1g 95% in stock $20.00 $14.00 -   +
5g 95% in stock $53.00 $37.00 -   +
10g 95% in stock $97.00 $68.00 -   +
25g 95% in stock $242.00 $170.00 -   +
100g 95% in stock $967.00 $677.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB64516
Chemical Name: 3-Bromo-6-chloro-2-fluoropyridine
CAS Number: 885952-18-1
Molecular Formula: C5H2BrClFN
Molecular Weight: 210.4315
MDL Number: MFCD06798230
SMILES: Clc1ccc(c(n1)F)Br

 

Computed Properties
Complexity: 103  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
XLogP3: 2.9  

 

 

Upstream Synthesis Route
  • 3-Bromo-6-chloro-2-fluoropyridine is a versatile chemical compound widely used in chemical synthesis. As a halogenated pyridine derivative, it serves as a valuable building block in the development of various pharmaceuticals, agrochemicals, and other fine chemicals. The unique combination of bromine, chlorine, and fluorine on the pyridine ring enables specific functionalization and selective reactions, making it a crucial intermediate in organic synthesis.In chemical synthesis, 3-Bromo-6-chloro-2-fluoropyridine is commonly employed as a key starting material for the preparation of heterocyclic compounds and complex organic molecules. Its halogen substituents facilitate diverse transformations such as nucleophilic substitution, cross-coupling reactions, and metal-catalyzed processes. This compound can participate in C-C bond formation, functional group modification, and stereoselective reactions, enabling chemists to access a wide range of structural motifs and stereochemical variations.Additionally, 3-Bromo-6-chloro-2-fluoropyridine plays a significant role in medicinal chemistry and drug discovery. By incorporating this pyridine derivative into molecular scaffolds, researchers can modulate the biological activity, pharmacokinetic properties, and target interactions of potential drug candidates. The unique reactivity and structural features of this compound make it a valuable tool for designing new therapeutic agents, agrochemicals, and materials with enhanced performance and tailored properties.
FEATURED PRODUCTS