Methyl N-Boc-4-piperidone-3-carboxylate
98%
- Product Code: 58933
Alias:
4-Oxopiperidine-1,3-dicarboxylic acid-1-tert-butyl-3-methyl ester; N-BOC-4-piperidone-3-methyl carboxylate; 1-tert-butoxycarbonyl-3- Methyl formate-4-piperidone; N-BOC-4-piperidone-3-methyl formate hydrochloride, N-BOC-3-methoxycarbonyl-4-piperidone hydrochloride; N- BOC-4-oxopiperidine-3-methyl carboxylate (P4M);
CAS:
161491-24-3
| Molecular Weight: | 257.28 g./mol | Molecular Formula: | C₁₂H₁₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08752608 | |
| Melting Point: | Boiling Point: | 350ºC | |
| Density: | 1.175g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of various biologically active compounds. It plays a key role in the development of pharmaceuticals, particularly in the synthesis of piperidine derivatives, which are important in drug discovery. The Boc (tert-butoxycarbonyl) group serves as a protective group for amines, enabling selective reactions during multi-step synthesis. It is commonly employed in the production of alkaloids, receptor ligands, and other therapeutic agents targeting neurological and cardiovascular systems. Additionally, its structure allows for further functionalization, making it valuable in medicinal chemistry research and the creation of complex molecules.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| Appearance | White-Pale Yellow Solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿960.00 |
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| 25.000 | 10-20 days | ฿3,980.00 |
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Methyl N-Boc-4-piperidone-3-carboxylate
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of various biologically active compounds. It plays a key role in the development of pharmaceuticals, particularly in the synthesis of piperidine derivatives, which are important in drug discovery. The Boc (tert-butoxycarbonyl) group serves as a protective group for amines, enabling selective reactions during multi-step synthesis. It is commonly employed in the production of alkaloids, receptor ligands, and other therapeutic agents targeting neurological and cardiovascular systems. Additionally, its structure allows for further functionalization, making it valuable in medicinal chemistry research and the creation of complex molecules.
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