N-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propanamide
95%
- Product Code: 83855
CAS:
2246698-15-5
| Molecular Weight: | 275.1584 g./mol | Molecular Formula: | C₁₅H₂₂BNO₃ |
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| EC Number: | MDL Number: | MFCD14585587 | |
| 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 like the Suzuki-Miyaura reaction, where it acts as a boronic ester derivative. Its structure allows it to serve as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and advanced materials. The tetramethyl-1,3,2-dioxaborolane group enhances stability and reactivity, making it suitable for constructing complex organic molecules. Additionally, it is employed in the development of bioactive compounds and in research focused on boron-based drug discovery. Its application extends to material science, where it contributes to the synthesis of polymers and organic electronic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $136.62 |
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| 0.250 | 10-20 days | $378.71 |
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| 1.000 | 10-20 days | $1,125.51 |
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N-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propanamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic ester derivative. Its structure allows it to serve as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and advanced materials. The tetramethyl-1,3,2-dioxaborolane group enhances stability and reactivity, making it suitable for constructing complex organic molecules. Additionally, it is employed in the development of bioactive compounds and in research focused on boron-based drug discovery. Its application extends to material science, where it contributes to the synthesis of polymers and organic electronic materials.
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