Methyl 4-bromo-3-hydroxythiophene-2-carboxylate
≥95%
- Product Code: 47466
CAS:
95201-93-7
| Molecular Weight: | 237.07 g./mol | Molecular Formula: | C₆H₅BrO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00052081 | |
| Melting Point: | 79-80°C | Boiling Point: | 247.9±35.0°C at 760 mmHg |
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and a hydroxyl group, makes it a valuable precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecular frameworks. Additionally, it serves as a key building block in the synthesis of thiophene derivatives, which are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Its ester functionality further allows for modifications, enabling the creation of diverse compounds with tailored properties for specific applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿585.00 |
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| 0.250 | 10-20 days | ฿1,197.00 |
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| 1.000 | 10-20 days | ฿1,638.00 |
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| 5.000 | 10-20 days | ฿6,507.00 |
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Methyl 4-bromo-3-hydroxythiophene-2-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and a hydroxyl group, makes it a valuable precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecular frameworks. Additionally, it serves as a key building block in the synthesis of thiophene derivatives, which are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Its ester functionality further allows for modifications, enabling the creation of diverse compounds with tailored properties for specific applications.
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