(R)-2-(((Benzyloxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid
97%
- Product Code: 54083
CAS:
27025-24-7
| Molecular Weight: | 295.29 g./mol | Molecular Formula: | C₁₄H₁₇NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191089 | |
| Melting Point: | Boiling Point: | 510.6°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, dry sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various peptide-based drugs and bioactive molecules. Its structure, featuring both a carboxyl group and a protected amino group, makes it suitable for use in solid-phase peptide synthesis (SPPS) and other peptide coupling reactions. Additionally, the benzyloxycarbonyl (Cbz) protecting group allows for selective deprotection, enabling the controlled assembly of complex peptide chains. This chemical is also employed in the development of enzyme inhibitors and receptor agonists, particularly in studies targeting neurological and metabolic disorders. Its versatility and stability make it a valuable tool in medicinal chemistry and drug discovery processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off white powder or crystals |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿250.00 |
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| 0.250 | 10-20 days | ฿330.00 |
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| 1.000 | 10-20 days | ฿710.00 |
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| 5.000 | 10-20 days | ฿2,620.00 |
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(R)-2-(((Benzyloxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various peptide-based drugs and bioactive molecules. Its structure, featuring both a carboxyl group and a protected amino group, makes it suitable for use in solid-phase peptide synthesis (SPPS) and other peptide coupling reactions. Additionally, the benzyloxycarbonyl (Cbz) protecting group allows for selective deprotection, enabling the controlled assembly of complex peptide chains. This chemical is also employed in the development of enzyme inhibitors and receptor agonists, particularly in studies targeting neurological and metabolic disorders. Its versatility and stability make it a valuable tool in medicinal chemistry and drug discovery processes.
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