tert-Butyl 4-(((benzyloxy)carbonyl)amino)-4-carbamoylpiperidine-1-carboxylate
97%
- Product Code: 119624
CAS:
288154-17-6
Molecular Weight: | 377.44 g./mol | Molecular Formula: | C₁₉H₂₇N₃O₅ |
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EC Number: | MDL Number: | MFCD17170923 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of piperidine derivatives. Its structure, featuring both carbamate and amide functionalities, makes it valuable for constructing complex molecules with potential therapeutic applications. Researchers often employ it in peptide chemistry and drug discovery projects, where it aids in the creation of compounds targeting neurological disorders, cancer, and infectious diseases. Its protective groups (tert-butyl and benzyloxycarbonyl) allow for selective deprotection, enabling precise modifications during multi-step synthetic processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿603.00 |
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0.250 | 10-20 days | ฿1,017.00 |
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1.000 | 10-20 days | ฿3,042.00 |
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tert-Butyl 4-(((benzyloxy)carbonyl)amino)-4-carbamoylpiperidine-1-carboxylate
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of piperidine derivatives. Its structure, featuring both carbamate and amide functionalities, makes it valuable for constructing complex molecules with potential therapeutic applications. Researchers often employ it in peptide chemistry and drug discovery projects, where it aids in the creation of compounds targeting neurological disorders, cancer, and infectious diseases. Its protective groups (tert-butyl and benzyloxycarbonyl) allow for selective deprotection, enabling precise modifications during multi-step synthetic processes.
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