(3R,5S)-rel-tert-Butyl 3,5-dimethylpiperazine-1-carboxylate
98%
- Product Code: 123390
CAS:
129779-30-2
| Molecular Weight: | 214.30 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06795911 | |
| Melting Point: | Boiling Point: | 279.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperazine ring, makes it valuable for developing drugs that target central nervous system disorders, cardiovascular diseases, and other therapeutic areas. It is often employed in the preparation of compounds with potential anti-inflammatory, antimicrobial, or antiviral properties. Additionally, its tert-butyl and carboxylate groups enhance its stability and reactivity, making it suitable for complex chemical transformations in drug development processes. The compound’s stereochemistry also allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects in medicinal applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless Or White To Yellow Solid Or Liquid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿340.00 |
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| 0.250 | 10-20 days | ฿460.00 |
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| 1.000 | 10-20 days | ฿690.00 |
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| 5.000 | 10-20 days | ฿2,090.00 |
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| 25.000 | 10-20 days | ฿6,830.00 |
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(3R,5S)-rel-tert-Butyl 3,5-dimethylpiperazine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperazine ring, makes it valuable for developing drugs that target central nervous system disorders, cardiovascular diseases, and other therapeutic areas. It is often employed in the preparation of compounds with potential anti-inflammatory, antimicrobial, or antiviral properties. Additionally, its tert-butyl and carboxylate groups enhance its stability and reactivity, making it suitable for complex chemical transformations in drug development processes. The compound’s stereochemistry also allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects in medicinal applications.
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