(R)-5-Amino-2-(((benzyloxy)carbonyl)(trityl)amino)-5-oxopentanoic acid
97%
- Product Code: 37703
CAS:
200625-96-3
| Molecular Weight: | 522.59 g./mol | Molecular Formula: | C₃₂H₃₀N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00237348 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. Its structure, featuring a trityl group and a benzyloxycarbonyl (Cbz) protecting group, ensures selective deprotection during the synthesis of complex peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and maintain the integrity of the peptide chain. Additionally, its chiral nature allows for the production of enantiomerically pure peptides, which is crucial in pharmaceutical research and development. The compound’s stability and compatibility with various coupling reagents make it a reliable choice for synthesizing biologically active peptides and peptidomimetics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,718.00 |
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| 5.000 | 10-20 days | ฿5,436.00 |
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| 10.000 | 10-20 days | ฿7,767.00 |
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(R)-5-Amino-2-(((benzyloxy)carbonyl)(trityl)amino)-5-oxopentanoic acid
This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. Its structure, featuring a trityl group and a benzyloxycarbonyl (Cbz) protecting group, ensures selective deprotection during the synthesis of complex peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and maintain the integrity of the peptide chain. Additionally, its chiral nature allows for the production of enantiomerically pure peptides, which is crucial in pharmaceutical research and development. The compound’s stability and compatibility with various coupling reagents make it a reliable choice for synthesizing biologically active peptides and peptidomimetics.
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