4-Chloro-5-fluoro-6-methoxy-2-methylpyrimidine
≥95%
- Product Code: 86131
CAS:
1383976-40-6
| Molecular Weight: | 176.58 g./mol | Molecular Formula: | C₆H₆ClFN₂O |
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| EC Number: | MDL Number: | MFCD23163182 | |
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| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structural features make it valuable in the development of drugs targeting specific biological pathways, particularly in the creation of kinase inhibitors. These inhibitors are often used in the treatment of cancers and other diseases where abnormal cell signaling plays a critical role. Additionally, its pyrimidine core is a common motif in medicinal chemistry, enabling researchers to modify and optimize drug candidates for improved efficacy and selectivity. The compound’s specific substitutions (chloro, fluoro, and methoxy groups) contribute to its reactivity and ability to interact with biological targets, making it a versatile building block in drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $47.46 |
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| 0.250 | 10-20 days | $116.17 |
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4-Chloro-5-fluoro-6-methoxy-2-methylpyrimidine
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structural features make it valuable in the development of drugs targeting specific biological pathways, particularly in the creation of kinase inhibitors. These inhibitors are often used in the treatment of cancers and other diseases where abnormal cell signaling plays a critical role. Additionally, its pyrimidine core is a common motif in medicinal chemistry, enabling researchers to modify and optimize drug candidates for improved efficacy and selectivity. The compound’s specific substitutions (chloro, fluoro, and methoxy groups) contribute to its reactivity and ability to interact with biological targets, making it a versatile building block in drug discovery.
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