5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
96%
- Product Code: 39750
CAS:
903550-12-9
| Molecular Weight: | 324.2989 g./mol | Molecular Formula: | C₁₅H₂₉BN₂O₃Si |
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| EC Number: | MDL Number: | MFCD09037502 | |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a pyrazole ring and a protected hydroxyl group, makes it valuable for constructing complex molecules in pharmaceutical and agrochemical research. The trimethylsilyl ethoxymethyl (SEM) protecting group enhances its stability during reactions, allowing for selective deprotection when needed. This compound is often employed in the development of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds in a controlled manner.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,628.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a pyrazole ring and a protected hydroxyl group, makes it valuable for constructing complex molecules in pharmaceutical and agrochemical research. The trimethylsilyl ethoxymethyl (SEM) protecting group enhances its stability during reactions, allowing for selective deprotection when needed. This compound is often employed in the development of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds in a controlled manner.
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