3-(Aminomethyl)benzeneboronic acid hydrochloride
95%
- Product Code: 66994
CAS:
352525-94-1
| Molecular Weight: | 187.43 g./mol | Molecular Formula: | C₇H₁₀BNO₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02093050 | |
| Melting Point: | 248-250°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key building block for creating complex biaryl structures. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a crucial intermediate in the development of enzyme inhibitors and receptor ligands, aiding in drug discovery and biochemical research. Its stability and reactivity also make it valuable in the design of sensors and probes for detecting specific biomolecules in diagnostic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $89.41 |
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| 1.000 | 10-20 days | $250.83 |
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3-(Aminomethyl)benzeneboronic acid hydrochloride
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key building block for creating complex biaryl structures. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a crucial intermediate in the development of enzyme inhibitors and receptor ligands, aiding in drug discovery and biochemical research. Its stability and reactivity also make it valuable in the design of sensors and probes for detecting specific biomolecules in diagnostic applications.
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