1-N-Boc-Pyrrolidin-2-ylboronic acid
97%
- Product Code: 91021
CAS:
149682-75-7
| Molecular Weight: | 215.06 g./mol | Molecular Formula: | C₉H₁₈BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 349.2°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. The Boc group provides protection for the amine functionality, allowing selective reactions to occur at the boronic acid site. This selectivity is crucial in constructing complex molecules with high precision. Additionally, it is employed in the development of bioactive compounds, where the pyrrolidine ring contributes to the desired pharmacological properties. Its stability and reactivity make it a valuable tool in medicinal chemistry for creating diverse molecular structures.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Pale-yellow to Yellow-brown solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿460.00 |
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| 1.000 | 10-20 days | ฿1,250.00 |
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| 5.000 | 10-20 days | ฿3,660.00 |
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| 25.000 | 10-20 days | ฿14,550.00 |
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1-N-Boc-Pyrrolidin-2-ylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. The Boc group provides protection for the amine functionality, allowing selective reactions to occur at the boronic acid site. This selectivity is crucial in constructing complex molecules with high precision. Additionally, it is employed in the development of bioactive compounds, where the pyrrolidine ring contributes to the desired pharmacological properties. Its stability and reactivity make it a valuable tool in medicinal chemistry for creating diverse molecular structures.
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