(3S,4S)-tert-Butyl 3-amino-4-methylpiperidine-1-carboxylate
≥95%
- Product Code: 113249
CAS:
1434126-96-1
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD24873235 | |
| Melting Point: | Boiling Point: | ||
| 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 an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its specific structure, featuring both amino and carboxylate groups, makes it a valuable building block for the development of complex molecules, particularly in the creation of drugs targeting neurological and cardiovascular disorders. Additionally, its chiral centers enable its use in the production of enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of many therapeutic agents. The compound is also employed in research settings for the development of novel chemical entities and in the study of structure-activity relationships (SAR) in drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿21,540.00 |
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| 0.250 | 10-20 days | ฿28,720.00 |
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| 1.000 | 10-20 days | ฿86,360.00 |
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(3S,4S)-tert-Butyl 3-amino-4-methylpiperidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its specific structure, featuring both amino and carboxylate groups, makes it a valuable building block for the development of complex molecules, particularly in the creation of drugs targeting neurological and cardiovascular disorders. Additionally, its chiral centers enable its use in the production of enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of many therapeutic agents. The compound is also employed in research settings for the development of novel chemical entities and in the study of structure-activity relationships (SAR) in drug discovery.
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