2-(4-((2-Bromophenoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 83784
CAS:
2246676-65-1
| Molecular Weight: | 389.09 g./mol | Molecular Formula: | C₁₉H₂₂BBrO₃ |
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| EC Number: | MDL Number: | MFCD31916473 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, especially in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a boronate group, makes it valuable for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The bromophenoxy moiety in its structure can also serve as a reactive site for further functionalization, enabling the creation of diverse chemical compounds. Its stability and reactivity make it a useful tool in medicinal chemistry for designing and synthesizing drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿3,078.00 |
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| 0.100 | 10-20 days | ฿6,156.00 |
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2-(4-((2-Bromophenoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis, especially in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a boronate group, makes it valuable for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The bromophenoxy moiety in its structure can also serve as a reactive site for further functionalization, enabling the creation of diverse chemical compounds. Its stability and reactivity make it a useful tool in medicinal chemistry for designing and synthesizing drug candidates.
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