(S)-tert-butyl 2-isopropylpiperazine-1-carboxylate
≥95%
- Product Code: 60169
CAS:
674792-05-3
| Molecular Weight: | 228.33 g./mol | Molecular Formula: | C₁₂H₂₄N₂O₂ |
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| EC Number: | MDL Number: | MFCD03787918 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both a piperazine ring and a tert-butyl group, makes it valuable for constructing active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting neurological and psychiatric disorders. The stereochemistry of the compound also allows for the creation of enantiomerically pure substances, which is crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it serves as a building block in organic synthesis for designing ligands and catalysts used in asymmetric synthesis, aiding in the production of chiral compounds. Its stability and reactivity further enhance its utility in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,575.00 |
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| 1.000 | 10-20 days | ฿5,427.00 |
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(S)-tert-butyl 2-isopropylpiperazine-1-carboxylate
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both a piperazine ring and a tert-butyl group, makes it valuable for constructing active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting neurological and psychiatric disorders. The stereochemistry of the compound also allows for the creation of enantiomerically pure substances, which is crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it serves as a building block in organic synthesis for designing ligands and catalysts used in asymmetric synthesis, aiding in the production of chiral compounds. Its stability and reactivity further enhance its utility in medicinal chemistry and drug discovery processes.
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