tert-Butyl (6-methylpiperidin-3-yl)carbamate
≥95%
- Product Code: 117639
CAS:
1150618-39-5
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD12031277 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring a piperidine ring and a tert-butyl carbamate group, makes it particularly valuable in the development of biologically active molecules, such as enzyme inhibitors and receptor modulators. The compound is often employed in the synthesis of drugs targeting neurological disorders, including those related to dopamine and serotonin pathways. Additionally, its stability and reactivity make it suitable for use in peptide coupling reactions and other complex chemical transformations. Researchers also leverage its properties in the design of prodrugs, which are inactive compounds that convert into active drugs within the body. Overall, it plays a crucial role in advancing medicinal chemistry and drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,013.00 |
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tert-Butyl (6-methylpiperidin-3-yl)carbamate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring a piperidine ring and a tert-butyl carbamate group, makes it particularly valuable in the development of biologically active molecules, such as enzyme inhibitors and receptor modulators. The compound is often employed in the synthesis of drugs targeting neurological disorders, including those related to dopamine and serotonin pathways. Additionally, its stability and reactivity make it suitable for use in peptide coupling reactions and other complex chemical transformations. Researchers also leverage its properties in the design of prodrugs, which are inactive compounds that convert into active drugs within the body. Overall, it plays a crucial role in advancing medicinal chemistry and drug discovery efforts.
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