4,4,5,5-tetramethyl-2-4-[(3-methylphenyl)methoxy]phenyl-1,3,2-dioxaborolane
95%
- Product Code: 45822
CAS:
1029439-14-2
| Molecular Weight: | 324.23 g./mol | Molecular Formula: | C₂₀H₂₅BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22493805 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. Its structure, featuring a dioxaborolane ring, makes it particularly useful in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the methoxy and methylphenyl groups enhances its reactivity and selectivity in these reactions, allowing for the efficient formation of carbon-carbon bonds. Additionally, it can serve as a precursor for the development of boron-based polymers and sensors, leveraging its stability and functional versatility. Its applications also extend to the field of medicinal chemistry, where it may be used in the design of boron-containing drugs, particularly in the development of protease inhibitors and other therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿64,062.00 |
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4,4,5,5-tetramethyl-2-4-[(3-methylphenyl)methoxy]phenyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. Its structure, featuring a dioxaborolane ring, makes it particularly useful in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the methoxy and methylphenyl groups enhances its reactivity and selectivity in these reactions, allowing for the efficient formation of carbon-carbon bonds. Additionally, it can serve as a precursor for the development of boron-based polymers and sensors, leveraging its stability and functional versatility. Its applications also extend to the field of medicinal chemistry, where it may be used in the design of boron-containing drugs, particularly in the development of protease inhibitors and other therapeutic agents.
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