4-Bromothiophene-2-sulfonylchloride
≥95%
- Product Code: 155089
CAS:
185329-76-4
| Molecular Weight: | 261.54 g./mol | Molecular Formula: | C₄H₂BrClO₂S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01763894 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, avoiding light |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules containing thiophene moieties. Its sulfonyl chloride group readily reacts with nucleophiles like amines and alcohols, enabling the formation of sulfonamides and sulfonate esters—common structural elements in drug design. It is also employed in materials science for constructing conjugated systems in organic semiconductors and functional polymers. The bromine substituent allows further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in building complex organic architectures.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,307.28 |
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| 0.250 | 10-20 days | $1,861.35 |
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4-Bromothiophene-2-sulfonylchloride
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules containing thiophene moieties. Its sulfonyl chloride group readily reacts with nucleophiles like amines and alcohols, enabling the formation of sulfonamides and sulfonate esters—common structural elements in drug design. It is also employed in materials science for constructing conjugated systems in organic semiconductors and functional polymers. The bromine substituent allows further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in building complex organic architectures.
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