Methyl 3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-6-fluoro-1H-indole-4-carboxylate
98%
- Product Code: 44222
CAS:
1408282-25-6
Molecular Weight: | 366.3425 g./mol | Molecular Formula: | C₂₀H₁₅FN₂O₄ |
---|---|---|---|
EC Number: | MDL Number: | MFCD30478789 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a fluoroindole moiety and a phthalimide group, makes it a valuable intermediate in the design of molecules with potential therapeutic properties. Researchers often employ it in the creation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its applications extend to the study of anti-inflammatory, anticancer, and neuroprotective agents, where its unique chemical framework can be modified to enhance efficacy and selectivity. Additionally, it serves as a building block in organic synthesis, enabling the exploration of new chemical spaces for drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
0.100 | 10-20 days | $327.27 |
+
-
|
Methyl 3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-6-fluoro-1H-indole-4-carboxylate
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a fluoroindole moiety and a phthalimide group, makes it a valuable intermediate in the design of molecules with potential therapeutic properties. Researchers often employ it in the creation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its applications extend to the study of anti-inflammatory, anticancer, and neuroprotective agents, where its unique chemical framework can be modified to enhance efficacy and selectivity. Additionally, it serves as a building block in organic synthesis, enabling the exploration of new chemical spaces for drug discovery.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :