N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propane-1-sulfonamide
95%
- Product Code: 50857
CAS:
2071707-87-2
| Molecular Weight: | 325.23 g./mol | Molecular Formula: | C₁₅H₂₄BNO₄S |
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| EC Number: | MDL Number: | MFCD31916461 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of biologically active molecules. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct complex organic frameworks. Additionally, it serves as a precursor in the development of sulfonamide-based drugs, which are known for their antimicrobial, anti-inflammatory, and anticancer properties. The compound's unique structure also makes it suitable for use in material science, particularly in the design of advanced polymers and coatings with specific functional properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $136.62 |
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| 0.250 | 10-20 days | $378.71 |
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| 1.000 | 10-20 days | $1,125.51 |
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N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propane-1-sulfonamide
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of biologically active molecules. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct complex organic frameworks. Additionally, it serves as a precursor in the development of sulfonamide-based drugs, which are known for their antimicrobial, anti-inflammatory, and anticancer properties. The compound's unique structure also makes it suitable for use in material science, particularly in the design of advanced polymers and coatings with specific functional properties.
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