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AB50017

1186403-17-7 | 3-Bromo-5-chlorophenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $6.00 $4.00 -   +
1g 95% in stock $7.00 $5.00 -   +
5g 95% in stock $11.00 $8.00 -   +
25g 95% in stock $46.00 $33.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB50017
Chemical Name: 3-Bromo-5-chlorophenylboronic acid
CAS Number: 1186403-17-7
Molecular Formula: C6H5BBrClO2
Molecular Weight: 235.2707
MDL Number: MFCD13189469
SMILES: Clc1cc(Br)cc(c1)B(O)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
  • (3-Bromo-5-chlorophenyl)boronic acid is a versatile reagent commonly used in organic and medicinal chemistry. This compound plays a crucial role in chemical synthesis as a key building block for creating complex organic molecules. Its unique structure makes it a valuable tool for researchers and chemists looking to develop new pharmaceuticals, agrochemicals, and materials.One prominent application of (3-Bromo-5-chlorophenyl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. In this widely used method, the boronic acid moiety of the compound undergoes a palladium-catalyzed cross-coupling with an organic halide or pseudohalide, leading to the formation of a new carbon-carbon bond. This process enables the efficient construction of biaryl and heteroaryl compounds, which are essential structural motifs in many biologically active molecules.Additionally, (3-Bromo-5-chlorophenyl)boronic acid can be incorporated into various chemical transformations such as Heck reactions, hydrogenation reactions, and Buchwald-Hartwig amination. By leveraging the reactivity of the boronic acid functionality, chemists can access a diverse array of substituted aryl compounds with tailored properties and functionalities.Overall, (3-Bromo-5-chlorophenyl)boronic acid serves as a valuable tool in the toolkit of synthetic chemists, enabling the efficient and precise construction of complex organic molecules with applications across diverse fields of chemistry and biomedicine.
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