AB55063
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $203.00 | $142.00 | - + | |
1g | 97% | in stock | $480.00 | $336.00 | - + | |
5g | 97% | in stock | $1,412.00 | $989.00 | - + | |
10g | 97% | in stock | $2,345.00 | $1,642.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB55063 |
Chemical Name: | 3-Picoline-4-boronic acid HCl |
CAS Number: | 1072952-40-9 |
Molecular Formula: | C6H9BClNO2 |
Molecular Weight: | 173.4052 |
MDL Number: | MFCD06659519 |
SMILES: | OB(c1ccncc1C)O.Cl |
Complexity: | 110 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 3 |
Rotatable Bond Count: | 1 |
3-Methylpyridin-4-yl)boronic acid hydrochloride is a versatile chemical compound widely utilized in organic synthesis. Its primary application lies in the field of cross-coupling reactions, such as Suzuki-Miyaura coupling, where it serves as a valuable boronic acid derivative for the formation of carbon-carbon bonds.In the realm of chemical synthesis, this compound acts as a key building block for the construction of various functionalized molecules, including pharmaceuticals, agrochemicals, and materials. By enabling the selective introduction of the (3-Methylpyridin-4-yl) functional group into target molecules, it facilitates the creation of complex structures with enhanced properties and biological activities.Furthermore, the hydrochloride form of (3-Methylpyridin-4-yl)boronic acid offers improved stability and solubility, making it particularly advantageous for use in aqueous reaction conditions. Its compatibility with a wide range of substrates and transition metal catalysts underscores its significance as a valuable tool in the synthesis of diverse organic compounds.Overall, the application of (3-Methylpyridin-4-yl)boronic acid hydrochloride in chemical synthesis enables researchers to access new molecules and advance their understanding of structure-activity relationships, paving the way for the development of novel materials and therapeutics.