(3R,4S)-tert-Butyl 3-amino-4-fluoropyrrolidine-1-carboxylate
95%
- Product Code: 113252
CAS:
1009075-48-2
| Molecular Weight: | 204.24 g./mol | Molecular Formula: | C₉H₁₇FN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18071735 | |
| Melting Point: | Boiling Point: | 266 °C | |
| Density: | 1.13 g/cm3 | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both amino and fluoro functional groups, makes it a valuable intermediate in the creation of biologically active molecules. It is often employed in the development of enzyme inhibitors, receptor modulators, and other therapeutic agents targeting various diseases, including neurological disorders and cancer. The tert-butyl group enhances its stability and solubility, facilitating its use in complex organic reactions. Additionally, its stereochemistry allows for the exploration of chiral-specific interactions in drug design, contributing to the development of more effective and selective medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,631.00 |
+
-
|
| 0.250 | 10-20 days | ฿14,670.00 |
+
-
|
| 1.000 | 10-20 days | ฿39,591.00 |
+
-
|
(3R,4S)-tert-Butyl 3-amino-4-fluoropyrrolidine-1-carboxylate
This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both amino and fluoro functional groups, makes it a valuable intermediate in the creation of biologically active molecules. It is often employed in the development of enzyme inhibitors, receptor modulators, and other therapeutic agents targeting various diseases, including neurological disorders and cancer. The tert-butyl group enhances its stability and solubility, facilitating its use in complex organic reactions. Additionally, its stereochemistry allows for the exploration of chiral-specific interactions in drug design, contributing to the development of more effective and selective medications.
| 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 :