N-(2,4-Dimethoxybenzyl)-5-fluoropyrimidin-2-amine
95%
- Product Code: 87765
CAS:
1354819-21-8
| Molecular Weight: | 263.27 g./mol | Molecular Formula: | C₁₃H₁₄FN₃O₂ |
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| EC Number: | MDL Number: | MFCD26158677 | |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring a fluoropyrimidine core, makes it valuable in the design of anticancer agents, as fluoropyrimidines are known for their role in disrupting DNA synthesis in rapidly dividing cells. Additionally, the dimethoxybenzyl group enhances its potential for binding to specific biological targets, making it useful in the development of drugs for neurological or inflammatory conditions. Researchers also explore its applications in creating fluorescent probes for biochemical assays, leveraging its unique chemical properties for detection and imaging purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,965.00 |
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| 0.250 | 10-20 days | ฿13,275.00 |
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N-(2,4-Dimethoxybenzyl)-5-fluoropyrimidin-2-amine
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring a fluoropyrimidine core, makes it valuable in the design of anticancer agents, as fluoropyrimidines are known for their role in disrupting DNA synthesis in rapidly dividing cells. Additionally, the dimethoxybenzyl group enhances its potential for binding to specific biological targets, making it useful in the development of drugs for neurological or inflammatory conditions. Researchers also explore its applications in creating fluorescent probes for biochemical assays, leveraging its unique chemical properties for detection and imaging purposes.
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