2-Tert-Butyl 6-Methyl 3,4-Dihydroisoquinoline-2,6(1H)-Dicarboxylate
95%
- Product Code: 83348
CAS:
170097-66-2
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275038 | |
| Melting Point: | Boiling Point: | 413.0±45.0 °C(Predicted) | |
| Density: | 1.154±0.06 g/cm3(Predicted) | Storage Condition: | Store at room temperature, away from light, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique dihydroisoquinoline core makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects. It is often employed in the preparation of alkaloid-like molecules, which are explored for their biological activities, including anti-inflammatory, anti-cancer, and neuroprotective properties. Additionally, its ester functional groups provide versatility for further chemical modifications, enabling researchers to tailor its properties for specific applications in drug discovery and development. Its stability and reactivity also make it a useful building block in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,080.00 |
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| 0.250 | 10-20 days | ฿1,800.00 |
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| 1.000 | 10-20 days | ฿5,400.00 |
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2-Tert-Butyl 6-Methyl 3,4-Dihydroisoquinoline-2,6(1H)-Dicarboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique dihydroisoquinoline core makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects. It is often employed in the preparation of alkaloid-like molecules, which are explored for their biological activities, including anti-inflammatory, anti-cancer, and neuroprotective properties. Additionally, its ester functional groups provide versatility for further chemical modifications, enabling researchers to tailor its properties for specific applications in drug discovery and development. Its stability and reactivity also make it a useful building block in medicinal chemistry and material science research.
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