tert-butyl (5S)-5-(tert-butylsulfinylamino)spiro[5,7-dihydrocyclopenta[b]pyridine-6,4'-piperidine]-1'-carboxylate
95%
- Product Code: 60168
CAS:
2377355-49-0
| Molecular Weight: | 407.5687 g./mol | Molecular Formula: | C₂₁H₃₃N₃O₃S |
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| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of complex molecules, particularly those targeting biological pathways. Its structure, featuring a spirocyclic framework and a sulfinyl group, makes it a valuable building block for designing drug candidates with enhanced stereochemical control. It is often employed in the development of small molecule inhibitors, especially for enzymes or receptors involved in diseases such as cancer, neurological disorders, or inflammatory conditions. The tert-butyl and sulfinyl groups contribute to the compound's stability and reactivity, facilitating its use in multi-step synthetic routes. Additionally, its piperidine moiety is advantageous for improving the pharmacokinetic properties of potential therapeutics, such as bioavailability and metabolic stability. Researchers leverage this compound to explore novel therapeutic agents with optimized efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £220.65 |
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| 0.500 | 10-20 days | £772.28 |
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tert-butyl (5S)-5-(tert-butylsulfinylamino)spiro[5,7-dihydrocyclopenta[b]pyridine-6,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of complex molecules, particularly those targeting biological pathways. Its structure, featuring a spirocyclic framework and a sulfinyl group, makes it a valuable building block for designing drug candidates with enhanced stereochemical control. It is often employed in the development of small molecule inhibitors, especially for enzymes or receptors involved in diseases such as cancer, neurological disorders, or inflammatory conditions. The tert-butyl and sulfinyl groups contribute to the compound's stability and reactivity, facilitating its use in multi-step synthetic routes. Additionally, its piperidine moiety is advantageous for improving the pharmacokinetic properties of potential therapeutics, such as bioavailability and metabolic stability. Researchers leverage this compound to explore novel therapeutic agents with optimized efficacy and selectivity.
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