(R)-Methyl 3-((tert-butoxycarbonyl)amino)butanoate
97%
- Product Code: 37753
CAS:
159877-47-1
| Molecular Weight: | 217.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03788463 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require chiral specificity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps in the controlled assembly of amino acids without unwanted side reactions. Additionally, it serves as an intermediate in the development of β-amino acid derivatives, which are important in designing drugs with enhanced metabolic stability and bioavailability. Its application is also seen in the preparation of compounds for biological studies, aiding in the exploration of enzyme interactions and receptor binding activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,530.00 |
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| 1.000 | 10-20 days | ฿3,843.00 |
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| 5.000 | 10-20 days | ฿11,592.00 |
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| 10.000 | 10-20 days | ฿19,341.00 |
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(R)-Methyl 3-((tert-butoxycarbonyl)amino)butanoate
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require chiral specificity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps in the controlled assembly of amino acids without unwanted side reactions. Additionally, it serves as an intermediate in the development of β-amino acid derivatives, which are important in designing drugs with enhanced metabolic stability and bioavailability. Its application is also seen in the preparation of compounds for biological studies, aiding in the exploration of enzyme interactions and receptor binding activities.
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