(R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(isopropyl)amino)butanoate
97%
- Product Code: 113473
CAS:
946161-16-6
| Molecular Weight: | 316.74 g./mol | Molecular Formula: | C₁₂H₁₇ClN₄O₄ |
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| EC Number: | MDL Number: | MFCD30471714 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a nitropyrimidine core and an ester functional group, makes it valuable for developing compounds with potential biological activity. In pharmaceuticals, it may be used in the creation of drugs targeting specific enzymes or receptors, particularly in areas like oncology or infectious diseases. In agrochemicals, it serves as a building block for designing pesticides or herbicides due to its reactivity and potential to disrupt biological processes in pests or weeds. Its chiral nature also allows for the development of enantiomerically pure products, which can enhance efficacy and reduce side effects in final applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿459.00 |
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| 0.250 | 10-20 days | ฿765.00 |
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| 1.000 | 10-20 days | ฿2,295.00 |
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(R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(isopropyl)amino)butanoate
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a nitropyrimidine core and an ester functional group, makes it valuable for developing compounds with potential biological activity. In pharmaceuticals, it may be used in the creation of drugs targeting specific enzymes or receptors, particularly in areas like oncology or infectious diseases. In agrochemicals, it serves as a building block for designing pesticides or herbicides due to its reactivity and potential to disrupt biological processes in pests or weeds. Its chiral nature also allows for the development of enantiomerically pure products, which can enhance efficacy and reduce side effects in final applications.
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