1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-3-oxo-1,3-dihydroisobenzofuran-5-carbonitrile
97%
- Product Code: 123796
CAS:
372941-54-3
Molecular Weight: | 338.38 g./mol | Molecular Formula: | C₂₀H₁₉FN₂O₂ |
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EC Number: | MDL Number: | MFCD18252485 | |
Melting Point: | 49-52 °C | Boiling Point: | 490.7±45.0 °C(Predicted) |
Density: | 1.25±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It is often employed in the development of pharmaceutical agents targeting neurological disorders, particularly those involving serotonin and dopamine pathways. Its structural features make it a suitable candidate for creating compounds with potential antidepressant or antipsychotic properties. Additionally, it is explored in the design of inhibitors for specific enzymes or receptors, contributing to drug discovery efforts for treating mental health conditions. Its fluorophenyl and nitrile groups enhance its binding affinity and metabolic stability, making it valuable in optimizing drug candidates.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿8,118.00 |
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0.250 | 10-20 days | ฿15,642.00 |
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1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-3-oxo-1,3-dihydroisobenzofuran-5-carbonitrile
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It is often employed in the development of pharmaceutical agents targeting neurological disorders, particularly those involving serotonin and dopamine pathways. Its structural features make it a suitable candidate for creating compounds with potential antidepressant or antipsychotic properties. Additionally, it is explored in the design of inhibitors for specific enzymes or receptors, contributing to drug discovery efforts for treating mental health conditions. Its fluorophenyl and nitrile groups enhance its binding affinity and metabolic stability, making it valuable in optimizing drug candidates.
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