benzyl 4-broMo-3-(1-hydroxyethyl)-5,6-dihydropyridine-1(2H)-carboxylate
97%(HPLC)
- Product Code: 50811
CAS:
1823808-97-4
| Molecular Weight: | 340.21 g./mol | Molecular Formula: | C₁₅H₁₈BrNO₃ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring a bromo group and a hydroxyl group, makes it a versatile building block for constructing pharmacologically active compounds. Researchers often employ it in the development of potential drug candidates, particularly in the creation of molecules with therapeutic properties targeting neurological disorders or infections. Additionally, its dihydropyridine core is of interest in medicinal chemistry for designing compounds that interact with calcium channels, which are critical in cardiovascular and neurological research. The compound’s functional groups also allow for further chemical modifications, enabling its use in the synthesis of diverse chemical libraries for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿9,000.00 |
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benzyl 4-broMo-3-(1-hydroxyethyl)-5,6-dihydropyridine-1(2H)-carboxylate
This compound is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring a bromo group and a hydroxyl group, makes it a versatile building block for constructing pharmacologically active compounds. Researchers often employ it in the development of potential drug candidates, particularly in the creation of molecules with therapeutic properties targeting neurological disorders or infections. Additionally, its dihydropyridine core is of interest in medicinal chemistry for designing compounds that interact with calcium channels, which are critical in cardiovascular and neurological research. The compound’s functional groups also allow for further chemical modifications, enabling its use in the synthesis of diverse chemical libraries for drug discovery and development.
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