2-(p-Tolylsulfonyl)-6-thia-2-azaspiro[2.5]octane
95%
- Product Code: 75164
CAS:
1207754-86-6
| Molecular Weight: | 283.41 g./mol | Molecular Formula: | C₁₃H₁₇NO₂S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22123258 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures. Its unique spirocyclic framework makes it valuable in the design and synthesis of bioactive compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic compounds, which are essential in the development of drugs targeting various diseases. Additionally, its sulfonyl and thia groups contribute to its reactivity, enabling its use in cross-coupling reactions and as a building block for creating molecules with potential therapeutic applications. Its role in medicinal chemistry is significant, particularly in the exploration of new drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿122,550.00 |
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| 1.000 | 10-20 days | ฿283,850.00 |
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2-(p-Tolylsulfonyl)-6-thia-2-azaspiro[2.5]octane
This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures. Its unique spirocyclic framework makes it valuable in the design and synthesis of bioactive compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic compounds, which are essential in the development of drugs targeting various diseases. Additionally, its sulfonyl and thia groups contribute to its reactivity, enabling its use in cross-coupling reactions and as a building block for creating molecules with potential therapeutic applications. Its role in medicinal chemistry is significant, particularly in the exploration of new drug candidates with improved efficacy and selectivity.
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