N-[4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzenesulfonamide
95%
- Product Code: 90746
CAS:
914606-88-5
| Molecular Weight: | 359.3 g./mol | Molecular Formula: | C₁₈H₂₂BNO₄S |
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| EC Number: | MDL Number: | NOMDL0579357 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it finds application in the development of sensor molecules due to its ability to interact with specific analytes, making it useful in diagnostic and analytical chemistry. Its sulfonamide moiety also contributes to its potential use in designing bioactive compounds, particularly in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿3,285.00 |
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| 0.250 | 10-20 days | ฿7,758.00 |
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| 1.000 | 10-20 days | ฿17,334.00 |
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N-[4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzenesulfonamide
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it finds application in the development of sensor molecules due to its ability to interact with specific analytes, making it useful in diagnostic and analytical chemistry. Its sulfonamide moiety also contributes to its potential use in designing bioactive compounds, particularly in medicinal chemistry research.
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