tert-butyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate
99%
- Product Code: 242149
CAS:
1425970-61-1
| Molecular Weight: | 323.24 g./mol | Molecular Formula: | C₁₇H₃₀BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14706665 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its piperidine core protected with a tert-butyloxycarbonyl (Boc) group allows for selective reactivity and stability during multi-step syntheses. It is especially valuable in the preparation of bioactive compounds where a substituted piperidine scaffold is required. The methylene linker between the boronate and the piperidine ring provides flexibility for further functionalization, making it a versatile building block in medicinal chemistry and drug development.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White solid |
| Purity (%) | 99-100% |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿460.00 |
+
-
|
| 500mg | 10-20 days | ฿1,520.00 |
+
-
|
| 1g | 10-20 days | ฿2,990.00 |
+
-
|
| 5g | 10-20 days | ฿10,770.00 |
+
-
|
| bulk | 10-20 days | ฿0.00 |
+
-
|
tert-butyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its piperidine core protected with a tert-butyloxycarbonyl (Boc) group allows for selective reactivity and stability during multi-step syntheses. It is especially valuable in the preparation of bioactive compounds where a substituted piperidine scaffold is required. The methylene linker between the boronate and the piperidine ring provides flexibility for further functionalization, making it a versatile building block in medicinal chemistry and drug development.
| 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 :