tert-Butyl 4-(((4-(4-amino-2-fluorophenoxy)-6-methoxyquinolin-7-yl)oxy)methyl)piperidine-1-carboxylate
97%
- Product Code: 46000
CAS:
929252-65-3
| Molecular Weight: | 497.56 g./mol | Molecular Formula: | C₂₇H₃₂FN₃O₅ |
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| EC Number: | MDL Number: | MFCD26386170 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as an intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors involved in disease pathways. Its structure, featuring a quinoline core and piperidine moiety, makes it a valuable scaffold for designing inhibitors or modulators of protein function. Researchers often employ it in the development of potential therapeutic agents for conditions such as cancer, inflammation, or neurological disorders. Its functional groups allow for further chemical modifications, enabling the creation of derivatives with optimized pharmacokinetic and pharmacodynamic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $27.54 |
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| 0.250 | 10-20 days | $46.17 |
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| 1.000 | 10-20 days | $139.06 |
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tert-Butyl 4-(((4-(4-amino-2-fluorophenoxy)-6-methoxyquinolin-7-yl)oxy)methyl)piperidine-1-carboxylate
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as an intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors involved in disease pathways. Its structure, featuring a quinoline core and piperidine moiety, makes it a valuable scaffold for designing inhibitors or modulators of protein function. Researchers often employ it in the development of potential therapeutic agents for conditions such as cancer, inflammation, or neurological disorders. Its functional groups allow for further chemical modifications, enabling the creation of derivatives with optimized pharmacokinetic and pharmacodynamic properties.
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