(9H-Fluoren-9-yl)methyl (2-bromoethyl)carbamate
≥95%
- Product Code: 195556
CAS:
340187-12-4
| Molecular Weight: | 346.22 g./mol | Molecular Formula: | C₁₇H₁₆BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00797866 | |
| Melting Point: | Boiling Point: | 491.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry seal |
Product Description:
Used primarily as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, especially in the development of protected amines for peptide and heterocyclic compound synthesis. The (9H-fluoren-9-yl)methyl (Fmoc) group acts as a protecting group for amines, allowing selective reaction at other functional sites during multi-step syntheses. Its stability under acidic conditions and easy removal under mild basic conditions (e.g., with piperidine) makes it highly valuable in solid-phase peptide synthesis. The bromoethyl moiety provides a reactive handle for further alkylation or cyclization reactions, enabling the construction of complex nitrogen-containing structures such as amino acids, drug candidates, and functionalized polymers. Commonly employed in medicinal chemistry for the preparation of targeted therapeutics, including kinase inhibitors and receptor modulators.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | ฿1,730.00 |
+
-
|
| 10g | 10-20 days | ฿2,770.00 |
+
-
|
| 25g | 10-20 days | ฿5,540.00 |
+
-
|
(9H-Fluoren-9-yl)methyl (2-bromoethyl)carbamate
Used primarily as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, especially in the development of protected amines for peptide and heterocyclic compound synthesis. The (9H-fluoren-9-yl)methyl (Fmoc) group acts as a protecting group for amines, allowing selective reaction at other functional sites during multi-step syntheses. Its stability under acidic conditions and easy removal under mild basic conditions (e.g., with piperidine) makes it highly valuable in solid-phase peptide synthesis. The bromoethyl moiety provides a reactive handle for further alkylation or cyclization reactions, enabling the construction of complex nitrogen-containing structures such as amino acids, drug candidates, and functionalized polymers. Commonly employed in medicinal chemistry for the preparation of targeted therapeutics, including kinase inhibitors and receptor modulators.
| 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 :