Tert-butyl (6,6-dimethoxy-3-oxocyclohexa-1,4-dien-1-YL)carbamate
95%
- Product Code: 84430
CAS:
175552-82-6
| Molecular Weight: | 269.29 g./mol | Molecular Formula: | C₁₃H₁₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24465646 | |
| Melting Point: | 130-131 °C | Boiling Point: | 376.2±42.0 °C(Predicted) |
| Density: | 1.15±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, where its structure is valuable for constructing specific functional groups or frameworks. The tert-butyl and carbamate moieties provide stability and reactivity, making it suitable for protecting amine groups during multi-step reactions. Additionally, its dimethoxy and oxo groups contribute to its versatility in cyclization and oxidation processes. This chemical is often employed in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Its role in facilitating controlled reactions underscores its importance in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,360.00 |
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| 0.250 | 10-20 days | ฿17,550.00 |
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| 1.000 | 10-20 days | ฿35,100.00 |
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Tert-butyl (6,6-dimethoxy-3-oxocyclohexa-1,4-dien-1-YL)carbamate
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, where its structure is valuable for constructing specific functional groups or frameworks. The tert-butyl and carbamate moieties provide stability and reactivity, making it suitable for protecting amine groups during multi-step reactions. Additionally, its dimethoxy and oxo groups contribute to its versatility in cyclization and oxidation processes. This chemical is often employed in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Its role in facilitating controlled reactions underscores its importance in medicinal chemistry and drug discovery.
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