6-Chloro-9-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-9H-purin-2-amine
99%
- Product Code: 61274
CAS:
848695-25-0
| Molecular Weight: | 318.77 g./mol | Molecular Formula: | C₁₄H₁₅ClN₆O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15528939 | |
| Melting Point: | 192-193℃ | Boiling Point: | |
| Density: | 1.50g/cm3 | Storage Condition: | -20℃ |
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 biologically active molecules. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for targeting specific pathways involved in diseases such as cancer and inflammatory disorders. Researchers leverage its purine core and functional groups to design compounds that can modulate enzyme activity, making it a significant component in drug discovery efforts. Additionally, its pyridine and purine moieties contribute to its potential in creating molecules with enhanced binding affinity and selectivity for therapeutic targets.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98.5-100 |
| Appearance | POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿1,080.00 |
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| 0.025 | 10-20 days | ฿3,240.00 |
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| 0.100 | 10-20 days | ฿6,552.00 |
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6-Chloro-9-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-9H-purin-2-amine
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for targeting specific pathways involved in diseases such as cancer and inflammatory disorders. Researchers leverage its purine core and functional groups to design compounds that can modulate enzyme activity, making it a significant component in drug discovery efforts. Additionally, its pyridine and purine moieties contribute to its potential in creating molecules with enhanced binding affinity and selectivity for therapeutic targets.
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