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AA82819

160591-91-3 | 4-Chloro-2-fluorophenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $6.00 $4.00 -   +
1g 97% in stock $7.00 $5.00 -   +
5g 97% in stock $18.00 $12.00 -   +
10g 97% in stock $30.00 $21.00 -   +
25g 97% in stock $43.00 $30.00 -   +
100g 97% in stock $170.00 $119.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA82819
Chemical Name: 4-Chloro-2-fluorophenylboronic acid
CAS Number: 160591-91-3
Molecular Formula: C6H5BClFO2
Molecular Weight: 174.3651
MDL Number: MFCD02684293
SMILES: Clc1ccc(c(c1)F)B(O)O

 

Computed Properties
Complexity: 136  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 4-Chloro-2-fluorophenylboronic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. As a key building block in organic chemistry, this compound plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 4-Chloro-2-fluorophenylboronic acid serves as a valuable precursor for the synthesis of biologically active molecules and functional materials. Its boronic acid functionality allows for easy cross-coupling reactions with a variety of organic substrates, enabling the formation of complex molecular structures with high efficiency. This compound is particularly valuable in Suzuki-Miyaura coupling reactions, where it can be employed to introduce the 4-chloro-2-fluorophenyl moiety into organic frameworks.Additionally, 4-Chloro-2-fluorophenylboronic acid is utilized in the development of coordination complexes and catalysts for organic transformations. Its unique chemical properties make it a suitable candidate for designing novel ligands and organometallic complexes that display enhanced reactivity and selectivity in various synthetic processes.Overall, the application of 4-Chloro-2-fluorophenylboronic acid in chemical synthesis underscores its significance as a valuable tool for constructing diverse molecular architectures and advancing the frontiers of organic chemistry.
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