(4-((4-Fluorobenzyl)oxy)phenyl)boronic acid
95%
- Product Code: 36812
CAS:
871125-82-5
| Molecular Weight: | 246.0420 g./mol | Molecular Formula: | C₁₃H₁₂BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07784403 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to react with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of bioactive molecules and in research focused on creating complex organic structures. Its fluorobenzyloxy group can enhance the compound's stability and reactivity in certain chemical environments, making it suitable for specialized synthetic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €21.61 |
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(4-((4-Fluorobenzyl)oxy)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to react with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of bioactive molecules and in research focused on creating complex organic structures. Its fluorobenzyloxy group can enhance the compound's stability and reactivity in certain chemical environments, making it suitable for specialized synthetic applications.
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