1-(tert-Butoxycarbonyl)-1,4-diazepane-5-carboxylic acid
95%
- Product Code: 39575
CAS:
1214824-64-2
| Molecular Weight: | 244.2875 g./mol | Molecular Formula: | C₁₁H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09752214 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a diazepane ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in medicinal chemistry. The Boc group can be easily removed under mild conditions, allowing for further functionalization of the molecule. Additionally, its carboxylic acid moiety enables coupling reactions, facilitating the creation of peptides or other amide-linked compounds. This compound is especially relevant in the development of central nervous system (CNS) drugs, as the diazepane scaffold is often found in molecules targeting neurological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | €193.04 |
+
-
|
1-(tert-Butoxycarbonyl)-1,4-diazepane-5-carboxylic acid
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a diazepane ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in medicinal chemistry. The Boc group can be easily removed under mild conditions, allowing for further functionalization of the molecule. Additionally, its carboxylic acid moiety enables coupling reactions, facilitating the creation of peptides or other amide-linked compounds. This compound is especially relevant in the development of central nervous system (CNS) drugs, as the diazepane scaffold is often found in molecules targeting neurological pathways.
| 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 :