2-(Acetoxymethyl)-6-chlorophenylboronic Acid Pinacol Ester
95%
- Product Code: 89685
| Molecular Weight: | 310.58 g./mol | Molecular Formula: | C₁₅H₂₀ClO₄B |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28101626 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent to form carbon-carbon bonds. This makes it essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions allow for efficient and selective transformations in multi-step synthetic processes. Additionally, it is employed in the synthesis of biologically active compounds, where its structural features contribute to the desired pharmacological properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿18,576.00 |
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| 1.000 | 10-20 days | ฿49,230.00 |
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2-(Acetoxymethyl)-6-chlorophenylboronic Acid Pinacol Ester
This compound is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent to form carbon-carbon bonds. This makes it essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions allow for efficient and selective transformations in multi-step synthetic processes. Additionally, it is employed in the synthesis of biologically active compounds, where its structural features contribute to the desired pharmacological properties.
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