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AD44993

352535-98-9 | 3-Bromo-2-chlorophenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $73.00 $51.00 -   +
1g 96% in stock $161.00 $113.00 -   +
5g 96% in stock $626.00 $439.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD44993
Chemical Name: 3-Bromo-2-chlorophenylboronic acid
CAS Number: 352535-98-9
Molecular Formula: C6H5BBrClO2
Molecular Weight: 235.2707
MDL Number: MFCD13184263
SMILES: OB(c1cccc(c1Cl)Br)O

 

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

 

 

Upstream Synthesis Route
  • The (3-Bromo-2-chlorophenyl)boronic acid is a versatile building block in chemical synthesis due to its unique properties. It is commonly used as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and materials science. This boronic acid derivative serves as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in a controlled and efficient manner. The presence of both bromine and chlorine substituents on the phenyl ring provides opportunities for further functionalization, leading to the creation of diverse molecular structures. Additionally, the boronic acid moiety facilitates compatibility with various transition metal catalysts, expanding its utility in organic transformations. Overall, the (3-Bromo-2-chlorophenyl)boronic acid is a crucial tool for synthetic chemists seeking to access complex molecules with specific chemical properties.
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