1-(2-((Tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
98%
- Product Code: 39157
CAS:
956907-34-9
| Molecular Weight: | 322.2200 g./mol | Molecular Formula: | C₁₆H₂₇BN₂O₄ |
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| EC Number: | MDL Number: | MFCD16294418 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group enables efficient Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tetrahydro-2H-pyran (THP) protecting group enhances its stability during synthetic processes, making it suitable for multi-step reactions. Its application extends to the development of complex molecules, including bioactive compounds and polymers, where precise control over molecular structure is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $134.85 |
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1-(2-((Tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group enables efficient Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tetrahydro-2H-pyran (THP) protecting group enhances its stability during synthetic processes, making it suitable for multi-step reactions. Its application extends to the development of complex molecules, including bioactive compounds and polymers, where precise control over molecular structure is essential.
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