(4-(1-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid
98%
- Product Code: 89217
CAS:
1704069-47-5
| Molecular Weight: | 334.23 g./mol | Molecular Formula: | C₁₇H₂₇BN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384346 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex molecules, including potential drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection, enabling further functionalization of the molecule. This versatility makes it a useful building block in the synthesis of compounds targeting various biological pathways, such as enzyme inhibitors or receptor modulators. Its application is particularly relevant in the design of small molecules for therapeutic purposes, including oncology, neuroscience, and infectious disease research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,348.63 |
+
-
|
(4-(1-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex molecules, including potential drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection, enabling further functionalization of the molecule. This versatility makes it a useful building block in the synthesis of compounds targeting various biological pathways, such as enzyme inhibitors or receptor modulators. Its application is particularly relevant in the design of small molecules for therapeutic purposes, including oncology, neuroscience, and infectious disease research.
| 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 :