(2-(Aminomethyl)-4-fluorophenyl)boronic acid hydrochloride
98%
- Product Code: 42796
CAS:
850568-02-4
| Molecular Weight: | 205.4200 g./mol | Molecular Formula: | C₇H₉BFNO₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04973742 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals, particularly those targeting enzyme inhibition or receptor modulation. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug development. The fluorine atom enhances its ability to interact with biological targets, making it valuable in the design of bioactive molecules. Additionally, it is employed in the development of diagnostic agents and imaging probes due to its specific reactivity and stability in aqueous environments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft60,022.56 |
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(2-(Aminomethyl)-4-fluorophenyl)boronic acid hydrochloride
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals, particularly those targeting enzyme inhibition or receptor modulation. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug development. The fluorine atom enhances its ability to interact with biological targets, making it valuable in the design of bioactive molecules. Additionally, it is employed in the development of diagnostic agents and imaging probes due to its specific reactivity and stability in aqueous environments.
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