(S)-3-((tert-butoxycarbonyl)amino)pentanoic acid
95%
- Product Code: 60700
CAS:
183990-48-9
| Molecular Weight: | 217.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275907 | |
| Melting Point: | 88-89 °C | Boiling Point: | 353.0±25.0 °C(Predicted) |
| Density: | 1.081±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
(S)-3-((tert-butoxycarbonyl)amino)pentanoic acid is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various bioactive compounds, particularly in the development of peptide-based drugs. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during multi-step synthetic processes, ensuring selective reactions. This compound is often employed in the synthesis of chiral molecules, where its stereochemistry plays a vital role in achieving the desired enantiomeric purity. Additionally, it finds utility in the production of amino acid derivatives and peptidomimetics, which are essential in drug discovery and medicinal chemistry. Its application extends to the study of enzyme inhibitors and receptor ligands, contributing to advancements in therapeutic agent development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $296.76 |
+
-
|
| 0.250 | 10-20 days | $446.08 |
+
-
|
| 1.000 | 10-20 days | $1,115.21 |
+
-
|
(S)-3-((tert-butoxycarbonyl)amino)pentanoic acid
(S)-3-((tert-butoxycarbonyl)amino)pentanoic acid is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various bioactive compounds, particularly in the development of peptide-based drugs. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during multi-step synthetic processes, ensuring selective reactions. This compound is often employed in the synthesis of chiral molecules, where its stereochemistry plays a vital role in achieving the desired enantiomeric purity. Additionally, it finds utility in the production of amino acid derivatives and peptidomimetics, which are essential in drug discovery and medicinal chemistry. Its application extends to the study of enzyme inhibitors and receptor ligands, contributing to advancements in therapeutic agent 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 | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :