1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine hydrochloride
97%
- Product Code: 244093
CAS:
1415794-62-5
| Molecular Weight: | 324.65 g./mol | Molecular Formula: | C₁₆H₂₆BClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17677250 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry, inert gas |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic halides and boronic acid derivatives. Its boronate ester group acts as a key coupling partner in the preparation of biaryl compounds, which are common structural motifs in pharmaceuticals and agrochemicals. The piperazine moiety enhances solubility and can serve as a linker in drug design, making this compound valuable in medicinal chemistry for building complex molecules. It is also employed in the development of functional materials, including conjugated polymers and organic electronic materials, due to its stability and reactivity under palladium catalysis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $171.46 |
+
-
|
| 1.000 | 10-20 days | $461.99 |
+
-
|
| 5.000 | 10-20 days | $1,617.76 |
+
-
|
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine hydrochloride
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic halides and boronic acid derivatives. Its boronate ester group acts as a key coupling partner in the preparation of biaryl compounds, which are common structural motifs in pharmaceuticals and agrochemicals. The piperazine moiety enhances solubility and can serve as a linker in drug design, making this compound valuable in medicinal chemistry for building complex molecules. It is also employed in the development of functional materials, including conjugated polymers and organic electronic materials, due to its stability and reactivity under palladium catalysis.
| 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 | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
$0.00
$0.00
Total :