Methyl 2-bromothiophene-3-carboxylate
95%
- Product Code: 206942
CAS:
76360-43-5
| Molecular Weight: | 221.07 g./mol | Molecular Formula: | C₆H₅BrO₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active thiophene derivatives. Its structure allows for selective functionalization, making it valuable in building complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form C–C bonds in drug discovery. Also utilized in the preparation of organic semiconductors and functional materials due to the electron-rich nature of the thiophene ring. Its ester and bromine groups offer dual reactivity sites for sequential transformations in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,330.00 |
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| 10g | 10-20 days | ฿9,410.00 |
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| 25g | 10-20 days | ฿23,460.00 |
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| 100g | 10-20 days | ฿83,200.00 |
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| 5g | 10-20 days | ฿5,120.00 |
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Methyl 2-bromothiophene-3-carboxylate
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active thiophene derivatives. Its structure allows for selective functionalization, making it valuable in building complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form C–C bonds in drug discovery. Also utilized in the preparation of organic semiconductors and functional materials due to the electron-rich nature of the thiophene ring. Its ester and bromine groups offer dual reactivity sites for sequential transformations in multi-step syntheses.
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