tert-Butyl 4-(3-(dimethylamino)acryloyl)piperidine-1-carboxylate
95%
- Product Code: 46194
CAS:
960201-86-9
| Molecular Weight: | 282.3785 g./mol | Molecular Formula: | C₁₅H₂₆N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08898850 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate. Its structure, featuring a piperidine ring and a dimethylamino acryloyl group, makes it valuable for constructing more complex molecules, particularly in the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cancer-related pathways, due to its ability to interact with biological receptors. Additionally, it serves as a building block in the preparation of compounds for studying structure-activity relationships (SAR) in medicinal chemistry. Its tert-butyl carboxylate group provides stability and facilitates further modifications during synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,988.00 |
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tert-Butyl 4-(3-(dimethylamino)acryloyl)piperidine-1-carboxylate
This compound is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate. Its structure, featuring a piperidine ring and a dimethylamino acryloyl group, makes it valuable for constructing more complex molecules, particularly in the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cancer-related pathways, due to its ability to interact with biological receptors. Additionally, it serves as a building block in the preparation of compounds for studying structure-activity relationships (SAR) in medicinal chemistry. Its tert-butyl carboxylate group provides stability and facilitates further modifications during synthetic processes.
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