Ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
97%
- Product Code: 118526
CAS:
301359-45-5
| Molecular Weight: | 310.80 g./mol | Molecular Formula: | C₁₄H₁₅ClN₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00492553 | |
| Melting Point: | Boiling Point: | 403.2±55.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pyrimidine derivatives, which are known for their diverse pharmacological properties. Researchers often employ it to create potential drug candidates targeting conditions such as inflammation, bacterial infections, and certain types of cancer. Additionally, its thioxo group and chlorophenyl moiety make it a versatile building block for designing compounds with enhanced binding affinity and specificity to biological targets. Its applications extend to agrochemical research, where it is explored for developing novel pesticides and herbicides due to its potential to disrupt specific enzymatic pathways in pests and weeds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,323.00 |
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| 0.250 | 10-20 days | ฿2,367.00 |
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| 1.000 | 10-20 days | ฿5,076.00 |
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Ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pyrimidine derivatives, which are known for their diverse pharmacological properties. Researchers often employ it to create potential drug candidates targeting conditions such as inflammation, bacterial infections, and certain types of cancer. Additionally, its thioxo group and chlorophenyl moiety make it a versatile building block for designing compounds with enhanced binding affinity and specificity to biological targets. Its applications extend to agrochemical research, where it is explored for developing novel pesticides and herbicides due to its potential to disrupt specific enzymatic pathways in pests and weeds.
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