(S)-2-(((Benzyloxy)carbonyl)amino)-6-(isopropylamino)hexanoic acid
97%
- Product Code: 53173
CAS:
218938-55-7
| Molecular Weight: | 322.40 g./mol | Molecular Formula: | C₁₇H₂₆N₂O₄ |
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| EC Number: | MDL Number: | MFCD01318752 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis as a building block for creating specific peptide sequences. Its structure allows it to act as a protected amino acid, ensuring selective reactivity during the synthesis process. The benzyloxycarbonyl (Cbz) group serves as a protective group for the amine functionality, preventing unwanted side reactions. The isopropylamino moiety contributes to the compound's unique properties, making it suitable for designing peptides with specific biological activities. It is often employed in research and development of pharmaceuticals, particularly in the study of peptide-based drugs, enzyme inhibitors, and receptor ligands. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds for medicinal chemistry applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,602.00 |
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| 0.250 | 10-20 days | ฿2,673.00 |
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| 1.000 | 10-20 days | ฿8,037.00 |
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(S)-2-(((Benzyloxy)carbonyl)amino)-6-(isopropylamino)hexanoic acid
This compound is primarily utilized in peptide synthesis as a building block for creating specific peptide sequences. Its structure allows it to act as a protected amino acid, ensuring selective reactivity during the synthesis process. The benzyloxycarbonyl (Cbz) group serves as a protective group for the amine functionality, preventing unwanted side reactions. The isopropylamino moiety contributes to the compound's unique properties, making it suitable for designing peptides with specific biological activities. It is often employed in research and development of pharmaceuticals, particularly in the study of peptide-based drugs, enzyme inhibitors, and receptor ligands. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds for medicinal chemistry applications.
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