(4AS,8aS,9S)-3-(benzyloxy)-4a-((tert-butyldimethylsilyl)oxy)-9-(dimethylamino)-8a,9-dihydronaphtho[2,3-d]isoxazole-4,5(4aH,8H)-dione
97%
- Product Code: 36956
CAS:
852821-06-8
| Molecular Weight: | 482.64 g./mol | Molecular Formula: | C₂₆H₃₄N₂O₅Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28023585 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structural features, including the benzyloxy and tert-butyldimethylsilyloxy groups, make it valuable for selective protection and deprotection strategies during multi-step synthetic processes. The dimethylamino group enhances its reactivity, enabling its use in the construction of nitrogen-containing heterocycles, which are common in bioactive compounds. Researchers often employ it in the synthesis of potential drug candidates targeting neurological or oncological disorders, leveraging its unique scaffold to explore structure-activity relationships. Additionally, its stability and functional groups allow for further modifications, making it a versatile tool in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,654.00 |
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| 0.250 | 10-20 days | ฿5,859.00 |
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| 1.000 | 10-20 days | ฿14,652.00 |
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(4AS,8aS,9S)-3-(benzyloxy)-4a-((tert-butyldimethylsilyl)oxy)-9-(dimethylamino)-8a,9-dihydronaphtho[2,3-d]isoxazole-4,5(4aH,8H)-dione
This compound is primarily utilized in organic synthesis as an intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structural features, including the benzyloxy and tert-butyldimethylsilyloxy groups, make it valuable for selective protection and deprotection strategies during multi-step synthetic processes. The dimethylamino group enhances its reactivity, enabling its use in the construction of nitrogen-containing heterocycles, which are common in bioactive compounds. Researchers often employ it in the synthesis of potential drug candidates targeting neurological or oncological disorders, leveraging its unique scaffold to explore structure-activity relationships. Additionally, its stability and functional groups allow for further modifications, making it a versatile tool in medicinal chemistry.
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