(3-((4-Methylpiperazin-1-yl)sulfonyl)phenyl)boronic acid
98%
- Product Code: 65441
CAS:
1704063-59-1
| Molecular Weight: | 284.14 g./mol | Molecular Formula: | C₁₁H₁₇BN₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384266 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of various therapeutic agents. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery. The compound’s structure, featuring a piperazine ring, enhances its potential in designing molecules with improved pharmacokinetic properties, such as increased solubility and bioavailability. It is particularly valuable in the synthesis of inhibitors targeting specific enzymes or receptors, contributing to the development of treatments for diseases like cancer, inflammation, and central nervous system disorders. Additionally, its sulfonyl group can enhance binding affinity to biological targets, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $1,308.42 |
+
-
|
(3-((4-Methylpiperazin-1-yl)sulfonyl)phenyl)boronic acid
Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of various therapeutic agents. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery. The compound’s structure, featuring a piperazine ring, enhances its potential in designing molecules with improved pharmacokinetic properties, such as increased solubility and bioavailability. It is particularly valuable in the synthesis of inhibitors targeting specific enzymes or receptors, contributing to the development of treatments for diseases like cancer, inflammation, and central nervous system disorders. Additionally, its sulfonyl group can enhance binding affinity to biological targets, making it a versatile building block in medicinal chemistry.
| 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 :