(3S,6S)-3,6-Diisopropylpiperazine-2,5-dione
≥95%
- Product Code: 36793
CAS:
19943-16-9
| Molecular Weight: | 198.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00190694 | |
| Melting Point: | Boiling Point: | 428.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
(3S,6S)-3,6-Diisopropylpiperazine-2,5-dione is primarily utilized in the field of organic synthesis as a key intermediate for the preparation of more complex chemical compounds. Its structure makes it valuable in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs and bioactive molecules. The compound is often employed in the creation of chiral building blocks, which are essential for producing enantiomerically pure substances. Additionally, it finds application in the study of stereochemistry and asymmetric synthesis, aiding researchers in understanding and controlling the spatial arrangement of atoms in molecules. Its role in the development of novel therapeutic agents and its contribution to advancing synthetic methodologies highlight its significance in chemical and pharmaceutical research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €175.18 |
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| 1.000 | 10-20 days | €522.36 |
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| 5.000 | 10-20 days | €1,581.34 |
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(3S,6S)-3,6-Diisopropylpiperazine-2,5-dione
(3S,6S)-3,6-Diisopropylpiperazine-2,5-dione is primarily utilized in the field of organic synthesis as a key intermediate for the preparation of more complex chemical compounds. Its structure makes it valuable in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs and bioactive molecules. The compound is often employed in the creation of chiral building blocks, which are essential for producing enantiomerically pure substances. Additionally, it finds application in the study of stereochemistry and asymmetric synthesis, aiding researchers in understanding and controlling the spatial arrangement of atoms in molecules. Its role in the development of novel therapeutic agents and its contribution to advancing synthetic methodologies highlight its significance in chemical and pharmaceutical research.
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