Ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylthio)pyrimidine-5-carboxylate
98%
- Product Code: 118771
CAS:
330785-81-4
| Molecular Weight: | 367.85 g./mol | Molecular Formula: | C₁₆H₁₈ClN₃O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17012695 | |
| Melting Point: | Boiling Point: | 514.9±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, protected from light and stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure is often modified to enhance drug efficacy, selectivity, and pharmacokinetic properties. Researchers explore its potential in designing novel therapeutic agents, especially for treating diseases where modulation of enzymatic activity or receptor signaling is crucial. Additionally, it may be investigated for its role in developing agrochemicals, contributing to the creation of new pesticides or herbicides with improved activity and safety profiles.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿288.00 |
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| 1.000 | 10-20 days | ฿657.00 |
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| 5.000 | 10-20 days | ฿2,160.00 |
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| 10.000 | 10-20 days | ฿3,240.00 |
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Ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylthio)pyrimidine-5-carboxylate
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure is often modified to enhance drug efficacy, selectivity, and pharmacokinetic properties. Researchers explore its potential in designing novel therapeutic agents, especially for treating diseases where modulation of enzymatic activity or receptor signaling is crucial. Additionally, it may be investigated for its role in developing agrochemicals, contributing to the creation of new pesticides or herbicides with improved activity and safety profiles.
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