3,3-dimethyl-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]butanamide
95%
- Product Code: 45704
CAS:
2246814-89-9
| Molecular Weight: | 317.23082 g./mol | Molecular Formula: | C₁₈H₂₈BNO₃ |
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| EC Number: | MDL Number: | MFCD31916414 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The butanamide moiety can also contribute to the compound's role in designing bioactive molecules, particularly in drug discovery efforts targeting enzyme inhibition or receptor modulation. Additionally, its boronate ester functionality is advantageous in the development of sensors and probes for detecting biological or chemical species.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $701.64 |
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| 1.000 | 10-20 days | $2,028.84 |
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3,3-dimethyl-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]butanamide
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The butanamide moiety can also contribute to the compound's role in designing bioactive molecules, particularly in drug discovery efforts targeting enzyme inhibition or receptor modulation. Additionally, its boronate ester functionality is advantageous in the development of sensors and probes for detecting biological or chemical species.
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