2-((6-Chloro-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)benzonitrile
98%
- Product Code: 42207
CAS:
865758-96-9
| Molecular Weight: | 275.69 g./mol | Molecular Formula: | C₁₃H₁₀ClN₃O₂ |
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| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the pharmaceutical and agrochemical industries due to its structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting enzyme inhibition or receptor modulation. Its pyrimidine core is often incorporated into molecules designed for antiviral, anticancer, or anti-inflammatory applications. In agrochemicals, it is used in the development of herbicides and pesticides, where its chemical structure helps in disrupting specific metabolic pathways in pests or weeds. Additionally, its nitrile group enhances its reactivity, making it a valuable building block in organic synthesis for creating more complex molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | ฿4,690.00 |
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2-((6-Chloro-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)benzonitrile
This chemical is primarily utilized in the pharmaceutical and agrochemical industries due to its structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting enzyme inhibition or receptor modulation. Its pyrimidine core is often incorporated into molecules designed for antiviral, anticancer, or anti-inflammatory applications. In agrochemicals, it is used in the development of herbicides and pesticides, where its chemical structure helps in disrupting specific metabolic pathways in pests or weeds. Additionally, its nitrile group enhances its reactivity, making it a valuable building block in organic synthesis for creating more complex molecules.
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