(4-Methoxy-3-(pyrrolidin-1-ylsulfonyl)-phenyl)boronic acid
98%
- Product Code: 89324
CAS:
874219-52-0
| Molecular Weight: | 285.12 g./mol | Molecular Formula: | C₁₁H₁₆BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08235070 | |
| Melting Point: | Boiling Point: | 521.7°C | |
| Density: | 1.41g/mL | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl compounds, which are essential in drug discovery. Additionally, it finds application in material science for designing advanced organic materials with specific electronic or optical properties. The methoxy and pyrrolidinylsulfonyl groups further enhance its reactivity and selectivity, making it a versatile building block in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $409.38 |
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(4-Methoxy-3-(pyrrolidin-1-ylsulfonyl)-phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl compounds, which are essential in drug discovery. Additionally, it finds application in material science for designing advanced organic materials with specific electronic or optical properties. The methoxy and pyrrolidinylsulfonyl groups further enhance its reactivity and selectivity, making it a versatile building block in synthetic chemistry.
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