2-[(Boc-amino)methyl]phenylboronic Acid Pinacol Ester
≥97%
- Product Code: 89766
CAS:
905300-76-7
| Molecular Weight: | 333.23 g./mol | Molecular Formula: | C₁₈H₂₈NO₄B |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07371552 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the Boc-protected amine group allows for selective deprotection, enabling further functionalization in multi-step synthetic processes. Its stability and reactivity make it a preferred choice in medicinal chemistry for developing drug candidates and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,212.00 |
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| 1.000 | 10-20 days | ฿12,222.00 |
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2-[(Boc-amino)methyl]phenylboronic Acid Pinacol Ester
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the Boc-protected amine group allows for selective deprotection, enabling further functionalization in multi-step synthetic processes. Its stability and reactivity make it a preferred choice in medicinal chemistry for developing drug candidates and bioactive compounds.
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