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Atomfair Thiophene, 2-(6-bromohexyl)- C10H15BrS
Description Thiophene, 2-(6-bromohexyl)- (CAS No. 116816-87-6) is a high-purity brominated thiophene derivative with the molecular formula C10H15BrS. This compound features a hexyl chain terminated by a bromine atom at the 6-position, attached to the 2-position of a thiophene ring, making it a versatile intermediate for organic synthesis and materials science applications. Its well-defined structure and reactive bromoalkyl group enable facile functionalization, particularly in polymer chemistry, conductive materials, and pharmaceutical research. Supplied as a clear to pale yellow liquid, this reagent is rigorously tested for quality, ensuring optimal performance in demanding laboratory and industrial processes. Store under inert conditions to maintain…
Description
Description
Thiophene, 2-(6-bromohexyl)- (CAS No. 116816-87-6) is a high-purity brominated thiophene derivative with the molecular formula C10H15BrS. This compound features a hexyl chain terminated by a bromine atom at the 6-position, attached to the 2-position of a thiophene ring, making it a versatile intermediate for organic synthesis and materials science applications. Its well-defined structure and reactive bromoalkyl group enable facile functionalization, particularly in polymer chemistry, conductive materials, and pharmaceutical research. Supplied as a clear to pale yellow liquid, this reagent is rigorously tested for quality, ensuring optimal performance in demanding laboratory and industrial processes. Store under inert conditions to maintain stability.
- CAS No: 116816-87-6
- Molecular Formula: C10H15BrS
- Molecular Weight: 247.20
- Exact Mass: 246.00778
- Monoisotopic Mass: 246.00778
- IUPAC Name: 2-(6-bromohexyl)thiophene
- SMILES: C1=CSC(=C1)CCCCCCBr
- Synonyms: Thiophene, 2-(6-bromohexyl)-, 116816-87-6, DTXSID10453104, DTXCID70403923, 2-(6-bromohexyl)thiophene
Application
2-(6-Bromohexyl)thiophene is widely used as a key building block in the synthesis of conjugated polymers for organic electronics, such as organic field-effect transistors (OFETs) and photovoltaic devices. Its bromoalkyl side chain allows for further modifications, including cross-coupling reactions and nucleophilic substitutions, facilitating the development of tailored materials. Researchers also employ this compound in the preparation of functionalized thiophene derivatives for drug discovery and agrochemical applications.
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