Methyl 4-chloro-3-hydroxythiophene-2-carboxylate
97%
- Product Code: 47158
CAS:
65449-59-4
| Molecular Weight: | 192.62 g./mol | Molecular Formula: | C₆H₅ClO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15071696 | |
| Melting Point: | Boiling Point: | 251.8°C at 760 mmHg | |
| Density: | 1.514g/cm3 | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and hydroxyl groups on a thiophene ring, makes it valuable for constructing complex molecules, particularly in the synthesis of biologically active compounds. It is often employed in the production of herbicides and fungicides, where its thiophene core contributes to the efficacy of the final product. Additionally, it serves as a building block in medicinal chemistry for designing drugs targeting specific enzymes or receptors, particularly in the development of anti-inflammatory and antimicrobial agents. Its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,285.00 |
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Methyl 4-chloro-3-hydroxythiophene-2-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and hydroxyl groups on a thiophene ring, makes it valuable for constructing complex molecules, particularly in the synthesis of biologically active compounds. It is often employed in the production of herbicides and fungicides, where its thiophene core contributes to the efficacy of the final product. Additionally, it serves as a building block in medicinal chemistry for designing drugs targeting specific enzymes or receptors, particularly in the development of anti-inflammatory and antimicrobial agents. Its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties.
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