6-Tert-Butyl 2-Methyl 7,8-Dihydro-1,6-Naphthyridine-2,6(5H)-Dicarboxylate
95%
- Product Code: 61445
CAS:
259809-47-7
| Molecular Weight: | 292.33 g./mol | Molecular Formula: | C₁₅H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09038018 | |
| Melting Point: | Boiling Point: | 432.9±45.0 °C(Predicted) | |
| Density: | 1.190±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique naphthyridine core makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It is often employed in the preparation of molecules that exhibit biological activity, such as inhibitors for specific enzymes or receptors. Additionally, its structural features allow it to be used in the design of ligands for catalytic systems, aiding in the development of efficient chemical reactions. The tert-butyl and methyl groups attached to the naphthyridine ring enhance its stability and reactivity, making it a versatile building block in medicinal chemistry and drug discovery research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £251.39 |
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| 0.250 | 10-20 days | £463.08 |
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| 1.000 | 10-20 days | £926.17 |
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6-Tert-Butyl 2-Methyl 7,8-Dihydro-1,6-Naphthyridine-2,6(5H)-Dicarboxylate
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique naphthyridine core makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It is often employed in the preparation of molecules that exhibit biological activity, such as inhibitors for specific enzymes or receptors. Additionally, its structural features allow it to be used in the design of ligands for catalytic systems, aiding in the development of efficient chemical reactions. The tert-butyl and methyl groups attached to the naphthyridine ring enhance its stability and reactivity, making it a versatile building block in medicinal chemistry and drug discovery research.
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