AB50587
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $5.00 | $4.00 | - + | |
1g | 98% | in stock | $10.00 | $7.00 | - + | |
5g | 98% | in stock | $37.00 | $26.00 | - + | |
10g | 98% | in stock | $74.00 | $52.00 | - + | |
25g | 98% | in stock | $175.00 | $123.00 | - + | |
100g | 98% | in stock | $699.00 | $490.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB50587 |
Chemical Name: | 1-(Tetrahydro-pyran-4-yl)-1H-pyrazole-4-boronic acid pinacol ester |
CAS Number: | 1040377-03-4 |
Molecular Formula: | C14H23BN2O3 |
Molecular Weight: | 278.155 |
MDL Number: | MFCD12033229 |
SMILES: | CC1(C)OB(OC1(C)C)c1cnn(c1)C1CCOCC1 |
Complexity: | 342 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 20 |
Hydrogen Bond Acceptor Count: | 4 |
Rotatable Bond Count: | 2 |
1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, or $name$, is a versatile compound widely utilized in chemical synthesis. This unique molecule serves as a key building block in the creation of structurally complex organic compounds. Due to its specific chemical structure, $name$ is particularly valuable in the formation of novel heterocyclic compounds with diverse applications in medicinal chemistry, material science, and agrochemical research.In chemical synthesis, 1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole acts as a valuable synthon, providing a convenient and efficient route for the introduction of both pyrazole and tetrahydropyran moieties into target molecules. The presence of boron within its structure further enhances its utility by enabling straightforward cross-coupling reactions to access a wide range of functionalized derivatives.By incorporating $name$ into synthetic pathways, chemists can access a diverse array of biologically active and structurally intricate compounds, making it an indispensable tool in the advancement of modern organic synthesis strategies.