4-(N,N-Dimethylsulfamoyl)phenylboronic acid
95%
- Product Code: 91004
CAS:
486422-59-7
| Molecular Weight: | 229.06 g./mol | Molecular Formula: | C₈H₁₂BNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659849 | |
| Melting Point: | 140-144°C | Boiling Point: | 410°C |
| Density: | 1.37g/mL | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis and medicinal chemistry as a versatile building block. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of protease inhibitors and other enzyme-targeting drugs. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in the synthesis of complex organic compounds. Additionally, it is utilized in the design of sensors and probes for detecting specific analytes, owing to its ability to interact with diols and other functional groups. Its sulfamoyl moiety further enhances its potential in drug discovery, as it can mimic transition states in enzymatic reactions, making it valuable for studying enzyme mechanisms and designing inhibitors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿873.00 |
+
-
|
| 1.000 | 10-20 days | ฿1,890.00 |
+
-
|
| 5.000 | 10-20 days | ฿8,244.00 |
+
-
|
4-(N,N-Dimethylsulfamoyl)phenylboronic acid
This compound is primarily used in organic synthesis and medicinal chemistry as a versatile building block. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of protease inhibitors and other enzyme-targeting drugs. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in the synthesis of complex organic compounds. Additionally, it is utilized in the design of sensors and probes for detecting specific analytes, owing to its ability to interact with diols and other functional groups. Its sulfamoyl moiety further enhances its potential in drug discovery, as it can mimic transition states in enzymatic reactions, making it valuable for studying enzyme mechanisms and designing inhibitors.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :