5-[(4-Benzyloxy)benzyl]-2,4-diaminopyrimidine
95%
- Product Code: 48216
CAS:
49873-11-2
| Molecular Weight: | 306.3617 g./mol | Molecular Formula: | C₁₈H₁₈N₄O |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 575.1 °C at 760 mmHg | |
| Density: | 1.252g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a pyrimidine core with amino and benzyloxybenzyl substituents, makes it a valuable building block for developing inhibitors targeting specific enzymes, particularly kinases. These inhibitors are crucial in the treatment of diseases such as cancer, where they can disrupt abnormal signaling pathways that promote tumor growth. Additionally, it serves as a precursor in the design of compounds with potential antiviral or antimicrobial properties, contributing to the development of new therapeutic options for infectious diseases. Its versatility in chemical modifications allows researchers to optimize its biological activity and selectivity for specific targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,722.00 |
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5-[(4-Benzyloxy)benzyl]-2,4-diaminopyrimidine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a pyrimidine core with amino and benzyloxybenzyl substituents, makes it a valuable building block for developing inhibitors targeting specific enzymes, particularly kinases. These inhibitors are crucial in the treatment of diseases such as cancer, where they can disrupt abnormal signaling pathways that promote tumor growth. Additionally, it serves as a precursor in the design of compounds with potential antiviral or antimicrobial properties, contributing to the development of new therapeutic options for infectious diseases. Its versatility in chemical modifications allows researchers to optimize its biological activity and selectivity for specific targets.
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