N-Methyl-N-[2-(4-morpholinyl)ethyl]-4-[[[[4-(trifluoromethyl)phenyl]amino]carbonyl]amino] benzamide
95%
- Product Code: 53359
CAS:
1005136-40-2
| Molecular Weight: | 450.45 g./mol | Molecular Formula: | C₂₂H₂₅F₃N₄O₃ |
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| Density: | Storage Condition: | 2-8°C |
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 various bioactive compounds, particularly those targeting specific enzymes or receptors involved in disease pathways. Its structure, featuring a trifluoromethylphenyl group and a morpholinyl moiety, makes it a valuable scaffold for developing potential therapeutic agents, especially in the areas of oncology and inflammation. Researchers often explore its derivatives for their inhibitory effects on certain proteins or signaling pathways, aiming to create novel drugs with enhanced efficacy and selectivity. Additionally, it may be used in biochemical assays to study molecular interactions and mechanisms of action in drug discovery projects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $2,621.80 |
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N-Methyl-N-[2-(4-morpholinyl)ethyl]-4-[[[[4-(trifluoromethyl)phenyl]amino]carbonyl]amino] benzamide
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting specific enzymes or receptors involved in disease pathways. Its structure, featuring a trifluoromethylphenyl group and a morpholinyl moiety, makes it a valuable scaffold for developing potential therapeutic agents, especially in the areas of oncology and inflammation. Researchers often explore its derivatives for their inhibitory effects on certain proteins or signaling pathways, aiming to create novel drugs with enhanced efficacy and selectivity. Additionally, it may be used in biochemical assays to study molecular interactions and mechanisms of action in drug discovery projects.
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