Ethyl 4-chloro-2,5-dimethylthieno[2,3-d]pyrimidine-6-carboxylate
95%
- Product Code: 83911
CAS:
148838-70-4
Molecular Weight: | 270.74 g./mol | Molecular Formula: | C₁₁H₁₁ClN₂O₂S |
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EC Number: | MDL Number: | MFCD00520812 | |
Melting Point: | Boiling Point: | 318.2±42.0 °C(Predicted) | |
Density: | 1.364±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting therapeutic applications. Its structure is often exploited in the design of molecules that interact with specific enzymes or receptors, making it valuable in the creation of potential drugs for treating diseases such as cancer, inflammation, or infections. Additionally, it may be employed in organic chemistry studies to explore novel reaction pathways or to develop new synthetic methodologies. Its unique thienopyrimidine core contributes to its significance in medicinal chemistry and drug discovery efforts.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿9,360.00 |
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0.250 | 10-20 days | ฿17,550.00 |
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1.000 | 10-20 days | ฿35,100.00 |
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Ethyl 4-chloro-2,5-dimethylthieno[2,3-d]pyrimidine-6-carboxylate
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting therapeutic applications. Its structure is often exploited in the design of molecules that interact with specific enzymes or receptors, making it valuable in the creation of potential drugs for treating diseases such as cancer, inflammation, or infections. Additionally, it may be employed in organic chemistry studies to explore novel reaction pathways or to develop new synthetic methodologies. Its unique thienopyrimidine core contributes to its significance in medicinal chemistry and drug discovery efforts.
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