(R)-Methyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride
95%
- Product Code: 230810
CAS:
1158-35-6
| Molecular Weight: | 330.81 g./mol | Molecular Formula: | C₁₅H₂₃ClN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00077026 | |
| Melting Point: | 110-113 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, inert atmosphere |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylate functionalities make it suitable for peptide coupling and solid-phase synthesis. Commonly employed in the preparation of enzyme inhibitors where stereochemistry is critical for activity. The benzyl carbamate (Cbz) group allows for selective deprotection under mild conditions, enabling stepwise assembly of complex peptides and peptidomimetics. Frequently utilized in research settings for structure-activity relationship studies and drug optimization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | ฿1,610.00 |
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| 25g | 10-20 days | ฿7,400.00 |
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(R)-Methyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylate functionalities make it suitable for peptide coupling and solid-phase synthesis. Commonly employed in the preparation of enzyme inhibitors where stereochemistry is critical for activity. The benzyl carbamate (Cbz) group allows for selective deprotection under mild conditions, enabling stepwise assembly of complex peptides and peptidomimetics. Frequently utilized in research settings for structure-activity relationship studies and drug optimization.
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