2-3-[(4-bromo-2-fluorophenoxy)methyl]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 41444
CAS:
2246736-67-2
| Molecular Weight: | 407.0816432 g./mol | Molecular Formula: | C₁₉H₂₁BBrFO₃ |
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| EC Number: | MDL Number: | MFCD31916481 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of drugs, enabling the creation of diverse aromatic compounds with potential therapeutic properties. Additionally, its specific structure, containing a bromo and fluoro substituent, allows for further functionalization, making it a versatile building block in medicinal chemistry research. It is also explored in material science for the synthesis of advanced organic materials, particularly those requiring precise molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | €205.38 |
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| 1.000 | 10-20 days | €593.60 |
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2-3-[(4-bromo-2-fluorophenoxy)methyl]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of drugs, enabling the creation of diverse aromatic compounds with potential therapeutic properties. Additionally, its specific structure, containing a bromo and fluoro substituent, allows for further functionalization, making it a versatile building block in medicinal chemistry research. It is also explored in material science for the synthesis of advanced organic materials, particularly those requiring precise molecular architectures.
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