2-chloro-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide
95%
- Product Code: 83502
CAS:
2057449-99-5
| Molecular Weight: | 295.56956 g./mol | Molecular Formula: | C₁₄H₁₉BClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32206450 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The boronate ester group in the molecule facilitates Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of complex organic molecules, including drug candidates and biologically active compounds. Additionally, its chloroacetamide moiety can be further functionalized, making it a versatile building block in medicinal chemistry and material science. Its application extends to the synthesis of boron-containing compounds, which are increasingly important in drug discovery and development due to their unique properties and potential therapeutic benefits.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿3,672.00 |
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| 0.100 | 10-20 days | ฿10,998.00 |
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2-chloro-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The boronate ester group in the molecule facilitates Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of complex organic molecules, including drug candidates and biologically active compounds. Additionally, its chloroacetamide moiety can be further functionalized, making it a versatile building block in medicinal chemistry and material science. Its application extends to the synthesis of boron-containing compounds, which are increasingly important in drug discovery and development due to their unique properties and potential therapeutic benefits.
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