(4-Methoxy-3-((4-methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
98%
- Product Code: 89320
CAS:
1704074-57-6
| Molecular Weight: | 313.1 g./mol | Molecular Formula: | C₁₃H₂₀BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400391 | |
| 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. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for developing new drug candidates and active ingredients. Additionally, it may be used in material science for synthesizing advanced polymers or functional materials. Its specific structure, with a methoxy and sulfonyl group, can enhance reactivity and selectivity in targeted chemical transformations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | €1,108.67 |
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(4-Methoxy-3-((4-methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for developing new drug candidates and active ingredients. Additionally, it may be used in material science for synthesizing advanced polymers or functional materials. Its specific structure, with a methoxy and sulfonyl group, can enhance reactivity and selectivity in targeted chemical transformations.
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