AA19213
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $14.00 | $10.00 | - + | |
250mg | 98% | in stock | $22.00 | $16.00 | - + | |
1g | 98% | in stock | $56.00 | $40.00 | - + | |
5g | 98% | in stock | $244.00 | $171.00 | - + | |
10g | 98% | in stock | $488.00 | $342.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA19213 |
Chemical Name: | 1,3-Dimethylpyrazole-4-boronic acid |
CAS Number: | 1146616-03-6 |
Molecular Formula: | C5H9BN2O2 |
Molecular Weight: | 139.9482 |
MDL Number: | MFCD18250638 |
SMILES: | Cn1cc(c(n1)C)B(O)O |
Complexity: | 122 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 1 |
The 1,3-dimethylpyrazole-4-boronic acid is a versatile reagent widely used in organic synthesis as a boronic acid derivative. Its unique structure consisting of a pyrazole ring and boronic acid moiety imparts valuable properties for various chemical reactions. In synthetic chemistry, this compound is often employed as a key building block in Suzuki-Miyaura cross-coupling reactions. By reacting with aryl or vinyl halides in the presence of a palladium catalyst, 1,3-dimethylpyrazole-4-boronic acid facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, this compound can participate in other transformation reactions such as borylation, arylation, and heteroatom functionalization, making it a valuable tool for the construction of diverse chemical scaffolds. Its ease of handling and compatibility with a wide range of functional groups further contribute to its utility in the field of chemical synthesis.