tert-butyl 4-(5-(tosyloxy)pentyl)piperidine-1-carboxylate
95%
- Product Code: 124587
CAS:
2102410-78-4
| Molecular Weight: | 425.58 g./mol | Molecular Formula: | C₂₂H₃₅NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31555363 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic applications. The tosyloxy group serves as a good leaving group, facilitating nucleophilic substitution reactions, while the tert-butyloxycarbonyl (Boc) group protects the piperidine nitrogen, allowing selective functionalization of the molecule. Its structure makes it valuable in constructing piperidine-based scaffolds, which are common in bioactive compounds targeting neurological and cardiovascular systems. Additionally, it can be used in peptide chemistry and the synthesis of heterocyclic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿19,305.00 |
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tert-butyl 4-(5-(tosyloxy)pentyl)piperidine-1-carboxylate
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic applications. The tosyloxy group serves as a good leaving group, facilitating nucleophilic substitution reactions, while the tert-butyloxycarbonyl (Boc) group protects the piperidine nitrogen, allowing selective functionalization of the molecule. Its structure makes it valuable in constructing piperidine-based scaffolds, which are common in bioactive compounds targeting neurological and cardiovascular systems. Additionally, it can be used in peptide chemistry and the synthesis of heterocyclic compounds.
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