(2R,5S)-tert-Butyl 2,5-dimethylpiperazine-1-carboxylate
≥95%
- Product Code: 113166
CAS:
309915-46-6
Molecular Weight: | 214.30 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
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EC Number: | MDL Number: | MFCD06797728 | |
Melting Point: | Boiling Point: | 280°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
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 chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular diseases. The tert-butyl and carboxylate groups enhance its stability and reactivity, facilitating its use in peptide coupling reactions and the creation of biologically active compounds. Additionally, it serves as a building block in the preparation of catalysts and ligands for asymmetric synthesis, aiding in the production of high-purity chiral substances. Its applications also extend to agrochemical research, where it contributes to the development of novel pesticides and herbicides.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | Ft2,909.01 |
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1.000 | 10-20 days | Ft5,818.02 |
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5.000 | 10-20 days | Ft27,926.49 |
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10.000 | 10-20 days | Ft54,204.54 |
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(2R,5S)-tert-Butyl 2,5-dimethylpiperazine-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 chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular diseases. The tert-butyl and carboxylate groups enhance its stability and reactivity, facilitating its use in peptide coupling reactions and the creation of biologically active compounds. Additionally, it serves as a building block in the preparation of catalysts and ligands for asymmetric synthesis, aiding in the production of high-purity chiral substances. Its applications also extend to agrochemical research, where it contributes to the development of novel pesticides and herbicides.
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