(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid
98%
- Product Code: 89186
CAS:
1704065-62-2
Molecular Weight: | 399.39 g./mol | Molecular Formula: | C₁₇H₃₀BNO₅SSi |
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EC Number: | MDL Number: | MFCD28384270 | |
Melting Point: | Boiling Point: | ||
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. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its tert-butyldimethylsilyl (TBDMS) protected hydroxyl group enhances stability during reactions, making it suitable for multi-step synthetic processes. It is often employed in pharmaceutical research and development for creating drug intermediates or active pharmaceutical ingredients (APIs). Additionally, its sulfonyl group can act as a directing group or participate in further functionalization, expanding its utility in medicinal chemistry and material science.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $1,931.10 |
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(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its tert-butyldimethylsilyl (TBDMS) protected hydroxyl group enhances stability during reactions, making it suitable for multi-step synthetic processes. It is often employed in pharmaceutical research and development for creating drug intermediates or active pharmaceutical ingredients (APIs). Additionally, its sulfonyl group can act as a directing group or participate in further functionalization, expanding its utility in medicinal chemistry and material science.
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