4,4,5,5-Tetramethyl-2-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)-1,3,2-dioxaborolane
97%
- Product Code: 78450
CAS:
889865-38-7
| Molecular Weight: | 304.19 g./mol | Molecular Formula: | C₁₇H₂₅BO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is widely used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester structure makes it valuable for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) and in material science for developing advanced polymers and electronic materials. Additionally, its stability and reactivity make it suitable for creating fine chemicals and agrochemicals. The tetrahydro-2H-pyran-2-yl (THP) protecting group enhances its solubility and handling properties during reactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Slightly pale yellow Crystal - Powder Solid |
| PURITY | 96.5 100% |
| MELTING POINT | 57 61? |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿460.00 |
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| 1.000 | 10-20 days | ฿950.00 |
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| 5.000 | 10-20 days | ฿3,200.00 |
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4,4,5,5-Tetramethyl-2-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)-1,3,2-dioxaborolane
This chemical is widely used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester structure makes it valuable for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) and in material science for developing advanced polymers and electronic materials. Additionally, its stability and reactivity make it suitable for creating fine chemicals and agrochemicals. The tetrahydro-2H-pyran-2-yl (THP) protecting group enhances its solubility and handling properties during reactions.
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