(R)-4-((Benzyloxy)carbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
≥95%
- Product Code: 71048
CAS:
138775-02-7
| Molecular Weight: | 364.39 g./mol | Molecular Formula: | C₁₈H₂₄N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179112 | |
| Melting Point: | Boiling Point: | 518.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various biologically active compounds, including peptide-based drugs. Its structure, featuring both benzyloxycarbonyl and tert-butoxycarbonyl protecting groups, makes it valuable in multi-step organic synthesis, where selective deprotection is required. Additionally, it is employed in the development of protease inhibitors and other therapeutic agents targeting specific enzymes or receptors. Its chiral nature also makes it useful in the preparation of enantiomerically pure substances, which are critical in drug development to ensure efficacy and reduce side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,115.00 |
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| 1.000 | 10-20 days | ฿5,337.00 |
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| 5.000 | 10-20 days | ฿16,434.00 |
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(R)-4-((Benzyloxy)carbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various biologically active compounds, including peptide-based drugs. Its structure, featuring both benzyloxycarbonyl and tert-butoxycarbonyl protecting groups, makes it valuable in multi-step organic synthesis, where selective deprotection is required. Additionally, it is employed in the development of protease inhibitors and other therapeutic agents targeting specific enzymes or receptors. Its chiral nature also makes it useful in the preparation of enantiomerically pure substances, which are critical in drug development to ensure efficacy and reduce side effects.
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