AB50017
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.
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 |
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 |
(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.