Ethyl 2-(2-chloroacetamido)-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate
95%
- Product Code: 58562
CAS:
203385-15-3
| Molecular Weight: | 287.76 g./mol | Molecular Formula: | C₁₂H₁₄ClNO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00436345 | |
| Melting Point: | Boiling Point: | 502.8±50.0 °C(Predicted) | |
| Density: | 1.391±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, especially those targeting therapeutic applications. Its structure, featuring a chloroacetamido group and a cyclopentathiophene moiety, makes it valuable for constructing complex heterocyclic compounds. These compounds are often explored for their potential in drug discovery, including the development of anti-inflammatory, anticancer, and antimicrobial agents. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse derivatives for biological screening and optimization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $492.06 |
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| 100mg | 10-20 days | $370.40 |
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| 1g | 10-20 days | $941.50 |
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Ethyl 2-(2-chloroacetamido)-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, especially those targeting therapeutic applications. Its structure, featuring a chloroacetamido group and a cyclopentathiophene moiety, makes it valuable for constructing complex heterocyclic compounds. These compounds are often explored for their potential in drug discovery, including the development of anti-inflammatory, anticancer, and antimicrobial agents. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse derivatives for biological screening and optimization.
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