(2S,3R)-2-((tert-butoxycarbonyl)(methyl)amino)-3-methoxybutanoic acid
95%
- Product Code: 104143
CAS:
136092-75-6
| Molecular Weight: | 247.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29978886 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various drugs, especially those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable for creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it helps in the introduction of specific amino acid residues into peptide chains, enhancing the biological activity of the resulting peptides. The tert-butoxycarbonyl (Boc) protecting group in the molecule is particularly useful in multi-step synthetic processes, as it can be easily removed under mild conditions without affecting other functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $714.32 |
+
-
|
| 0.250 | 10-20 days | $1,208.85 |
+
-
|
| 1.000 | 10-20 days | $2,417.71 |
+
-
|
(2S,3R)-2-((tert-butoxycarbonyl)(methyl)amino)-3-methoxybutanoic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various drugs, especially those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable for creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it helps in the introduction of specific amino acid residues into peptide chains, enhancing the biological activity of the resulting peptides. The tert-butoxycarbonyl (Boc) protecting group in the molecule is particularly useful in multi-step synthetic processes, as it can be easily removed under mild conditions without affecting other functional groups.
| 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 :