AA01799
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $58.00 | $41.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA01799 |
Chemical Name: | 2-Chloro-6-isopropylpyridine-3-boronic acid |
CAS Number: | 1003043-37-5 |
Molecular Formula: | C8H11BClNO2 |
Molecular Weight: | 199.4424 |
MDL Number: | MFCD08274472 |
SMILES: | CC(c1ccc(c(n1)Cl)B(O)O)C |
Complexity: | 168 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 2 |
(2-Chloro-6-isopropylpyridin-3-yl)boronic acid is a versatile chemical compound commonly utilized in chemical synthesis due to its unique properties and reactivity. This boronic acid derivative serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, (2-Chloro-6-isopropylpyridin-3-yl)boronic acid is often employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions. This reaction mechanism involves the coupling of an aryl or vinyl boronic acid with an organic halide or pseudohalide in the presence of a palladium catalyst. The resulting product is a biaryl or alkenyl compound, which is commonly found in many pharmaceuticals and fine chemicals.Additionally, this compound can act as a ligand in transition metal-catalyzed coupling reactions, enabling efficient carbon-carbon bond formation. Its ability to form stable complexes with transition metals enhances catalytic activity and selectivity in various organic transformations.Furthermore, (2-Chloro-6-isopropylpyridin-3-yl)boronic acid can participate in direct C-H functionalization reactions, facilitating the direct introduction of functional groups onto aromatic systems. This enables the rapid and efficient synthesis of complex molecules with diverse chemical properties.Overall, the application of (2-Chloro-6-isopropylpyridin-3-yl)boronic acid in chemical synthesis represents a significant contribution to the field of organic chemistry, offering a wide range of opportunities for the construction of novel and valuable compounds.