(S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid
≥95%
- Product Code: 113167
CAS:
1033713-11-9
| Molecular Weight: | 244.24 g./mol | Molecular Formula: | C₁₀H₁₆N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10698231 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the production of peptide-based drugs, where it is often employed to introduce specific structural features into the peptide chain. Its tert-butoxycarbonyl (Boc) protecting group is particularly valuable in peptide synthesis, as it can be selectively removed under mild acidic conditions without affecting other functional groups. Additionally, the compound is used in the development of protease inhibitors and other therapeutic agents targeting enzymatic pathways. Its chiral nature also makes it suitable for the creation of enantiomerically pure compounds, which are essential in drug development to ensure efficacy and reduce side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,593.00 |
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| 0.250 | 10-20 days | ฿3,069.00 |
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| 1.000 | 10-20 days | ฿9,711.00 |
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(S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the production of peptide-based drugs, where it is often employed to introduce specific structural features into the peptide chain. Its tert-butoxycarbonyl (Boc) protecting group is particularly valuable in peptide synthesis, as it can be selectively removed under mild acidic conditions without affecting other functional groups. Additionally, the compound is used in the development of protease inhibitors and other therapeutic agents targeting enzymatic pathways. Its chiral nature also makes it suitable for the creation of enantiomerically pure compounds, which are essential in drug development to ensure efficacy and reduce side effects.
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