3-(2-Bromoacetamido)phenylboronic acid, pinacol ester
95%
- Product Code: 83506
CAS:
2096331-74-5
| Molecular Weight: | 340.02 g./mol | Molecular Formula: | C₁₄H₁₉BBrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18783180 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, its bromoacetamido moiety allows for further functionalization, making it a versatile building block in medicinal chemistry for designing biologically active compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,589.00 |
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| 1.000 | 10-20 days | ฿14,436.00 |
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3-(2-Bromoacetamido)phenylboronic acid, pinacol ester
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, its bromoacetamido moiety allows for further functionalization, making it a versatile building block in medicinal chemistry for designing biologically active compounds.
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