tert-Butyl N-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)propyl]carbamate
95%
- Product Code: 65474
CAS:
1850305-80-4
| Molecular Weight: | 285.19 g./mol | Molecular Formula: | C₁₄H₂₈BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22383765 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas |
Product Description:
This chemical is widely used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds. Its primary application lies in the field of medicinal chemistry, where it serves as a building block for the development of pharmaceutical agents, especially those targeting protease enzymes and other biologically relevant molecules. The tetramethyl-1,3,2-dioxaborolane group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery and materials science. Additionally, it is utilized in the synthesis of boron neutron capture therapy (BNCT) agents, which are used in cancer treatment. The tert-butyl carbamate group provides stability and protection for amines during multi-step synthetic processes, making it a versatile reagent in complex organic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,214.00 |
+
-
|
| 0.250 | 10-20 days | ฿4,644.00 |
+
-
|
| 1.000 | 10-20 days | ฿10,332.00 |
+
-
|
tert-Butyl N-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)propyl]carbamate
This chemical is widely used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds. Its primary application lies in the field of medicinal chemistry, where it serves as a building block for the development of pharmaceutical agents, especially those targeting protease enzymes and other biologically relevant molecules. The tetramethyl-1,3,2-dioxaborolane group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery and materials science. Additionally, it is utilized in the synthesis of boron neutron capture therapy (BNCT) agents, which are used in cancer treatment. The tert-butyl carbamate group provides stability and protection for amines during multi-step synthetic processes, making it a versatile reagent in complex organic transformations.
| 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 :