Dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
97%
- Product Code: 115516
CAS:
21829-09-4
| Molecular Weight: | 346.34 g./mol | Molecular Formula: | C₁₇H₁₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00375648 | |
| Melting Point: | Boiling Point: | 493.1°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of dihydropyridine derivatives, which are known for their therapeutic potential. Specifically, it is used in the development of calcium channel blockers, a class of drugs that are effective in treating cardiovascular conditions such as hypertension and angina. Additionally, its structural framework is explored in the design of compounds with potential antioxidant, anti-inflammatory, and neuroprotective properties. Researchers also investigate its role in organic synthesis for creating complex molecules with diverse biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,367.00 |
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| 0.250 | 10-20 days | ฿3,942.00 |
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| 1.000 | 10-20 days | ฿11,826.00 |
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Dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of dihydropyridine derivatives, which are known for their therapeutic potential. Specifically, it is used in the development of calcium channel blockers, a class of drugs that are effective in treating cardiovascular conditions such as hypertension and angina. Additionally, its structural framework is explored in the design of compounds with potential antioxidant, anti-inflammatory, and neuroprotective properties. Researchers also investigate its role in organic synthesis for creating complex molecules with diverse biological activities.
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