4-Chloro-5-fluoro-2-(n-propyl-d7)-pyrimidine
95%
- Product Code: 46681
CAS:
1185317-83-2
| Molecular Weight: | 181.646355646 g./mol | Molecular Formula: | C₇HClD₇FN₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
4-Chloro-5-fluoro-2-(n-propyl-d7)-pyrimidine is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of deuterated compounds. Its deuterated propyl group makes it a valuable tool for studying drug metabolism and pharmacokinetics, as deuterium substitution can slow down the breakdown of molecules, allowing researchers to track and analyze the behavior of drugs in biological systems more effectively. This compound is often employed in the creation of labeled analogs of active pharmaceutical ingredients, aiding in the identification of metabolites and the understanding of metabolic pathways. Additionally, it serves as a building block in the design of novel therapeutic agents, especially in the development of antiviral and anticancer drugs, where pyrimidine derivatives play a significant role. Its use in isotopic labeling also supports advancements in nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry, enhancing the precision of analytical techniques in drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿7,120.00 |
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| 0.005 | 10-20 days | ฿22,660.00 |
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4-Chloro-5-fluoro-2-(n-propyl-d7)-pyrimidine
4-Chloro-5-fluoro-2-(n-propyl-d7)-pyrimidine is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of deuterated compounds. Its deuterated propyl group makes it a valuable tool for studying drug metabolism and pharmacokinetics, as deuterium substitution can slow down the breakdown of molecules, allowing researchers to track and analyze the behavior of drugs in biological systems more effectively. This compound is often employed in the creation of labeled analogs of active pharmaceutical ingredients, aiding in the identification of metabolites and the understanding of metabolic pathways. Additionally, it serves as a building block in the design of novel therapeutic agents, especially in the development of antiviral and anticancer drugs, where pyrimidine derivatives play a significant role. Its use in isotopic labeling also supports advancements in nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry, enhancing the precision of analytical techniques in drug discovery.
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