tert-butyl (3aR,8bS)-2,2-dioxo-4,8b-dihydro-3aH-indeno[1,2-d]oxathiazole-1-carboxylate
≥97%
- Product Code: 233162
CAS:
1091606-66-4
| Molecular Weight: | 311.35 g./mol | Molecular Formula: | C₁₄H₁₇NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17018784 | |
| Melting Point: | 139.0-140.2 °C | Boiling Point: | 415.7±55.0 °C(Predicted) |
| Density: | 1.361±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, inert gas |
Product Description:
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its rigid indeno-oxathiazole scaffold with defined stereochemistry makes it valuable for asymmetric synthesis and development of enzyme inhibitors. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in protease or kinase inhibitor programs. The tert-butyl carbamate-protected structure allows for selective deprotection and further functionalization, enabling its use in multi-step synthetic routes for drug candidates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿14,290.00 |
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| 1g | 10-20 days | ฿42,890.00 |
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tert-butyl (3aR,8bS)-2,2-dioxo-4,8b-dihydro-3aH-indeno[1,2-d]oxathiazole-1-carboxylate
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its rigid indeno-oxathiazole scaffold with defined stereochemistry makes it valuable for asymmetric synthesis and development of enzyme inhibitors. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in protease or kinase inhibitor programs. The tert-butyl carbamate-protected structure allows for selective deprotection and further functionalization, enabling its use in multi-step synthetic routes for drug candidates.
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