(1S)-tert-Butyl 6-bromo-1-(1,1-dimethylethylsulfinamido)-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxylate
97%
- Product Code: 123598
CAS:
2377355-25-2
| Molecular Weight: | 485.48 g./mol | Molecular Formula: | C₂₂H₃₃BrN₂O₃S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 563.5±60.0 °C(Predicted) | |
| Density: | 1.36±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of pharmaceutical agents. Its structure, featuring a spirocyclic indene-piperidine core, is particularly valuable in the design of molecules with potential biological activity. The tert-butyl and sulfinamide groups enhance its stability and reactivity, making it suitable for use in complex multi-step synthetic routes. It is often employed in the preparation of compounds targeting neurological disorders, such as Alzheimer's disease or Parkinson's disease, due to its ability to modulate specific receptors or enzymes in the central nervous system. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,788.00 |
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| 1.000 | 10-20 days | ฿11,970.00 |
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(1S)-tert-Butyl 6-bromo-1-(1,1-dimethylethylsulfinamido)-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of pharmaceutical agents. Its structure, featuring a spirocyclic indene-piperidine core, is particularly valuable in the design of molecules with potential biological activity. The tert-butyl and sulfinamide groups enhance its stability and reactivity, making it suitable for use in complex multi-step synthetic routes. It is often employed in the preparation of compounds targeting neurological disorders, such as Alzheimer's disease or Parkinson's disease, due to its ability to modulate specific receptors or enzymes in the central nervous system. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.
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