4-(4-Amino-3-fluorophenoxy)-N-methylpicolinamide
＞95%
- Product Code: 66338
Alias:
4-(4-amino-3-fluorophenoxy)pyridine-2-carboxylic acid methylamine; 4-(4-amino-3-fluorophenoxy)-N-methyl-2-pyridinecarboxamide;
CAS:
757251-39-1
| Molecular Weight: | 261.25 g./mol | Molecular Formula: | C₁₃H₁₂FN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09033852 | |
| Melting Point: | Boiling Point: | 459.8ºC at 760 mmHg | |
| Density: | 1.305g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of tyrosine kinase inhibitors, which are crucial in targeted cancer therapies. By acting on specific signaling pathways, these inhibitors can effectively halt the proliferation of cancer cells. Additionally, the presence of both amino and fluorine groups in the molecule enhances its binding affinity to biological targets, making it a versatile building block for designing drugs with improved efficacy and selectivity. Researchers also explore its potential in creating compounds for treating inflammatory diseases and other conditions where kinase modulation is beneficial.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,980.00 |
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4-(4-Amino-3-fluorophenoxy)-N-methylpicolinamide
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of tyrosine kinase inhibitors, which are crucial in targeted cancer therapies. By acting on specific signaling pathways, these inhibitors can effectively halt the proliferation of cancer cells. Additionally, the presence of both amino and fluorine groups in the molecule enhances its binding affinity to biological targets, making it a versatile building block for designing drugs with improved efficacy and selectivity. Researchers also explore its potential in creating compounds for treating inflammatory diseases and other conditions where kinase modulation is beneficial.
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