Description

1,6-Bis(5-(trimethylstannyl)thiophen-2-yl)hexane (CAS No. 1884354-21-5) is a highly specialized organotin compound with the molecular formula C₂₀H₃₄S₂Sn₂. This compound features a hexane backbone symmetrically substituted with thiophene rings, each bearing a trimethylstannyl group at the 5-position. Its precise IUPAC name is trimethyl-[5-[6-(5-trimethylstannylthiophen-2-yl)hexyl]thiophen-2-yl]stannane. This product is meticulously synthesized for advanced applications in materials science, particularly in the development of conductive polymers and organic electronic devices. It is available in high purity grades suitable for research and industrial use, with strict quality control to ensure consistency and performance.

Properties

• CAS Number: 1884354-21-5
• Complexity: 337
• IUPAC Name: trimethyl-[5-[6-(5-trimethylstannyl-2-thienyl)hexyl]-2-thienyl]stannane
• InChI: InChI=1S/C14H16S2.6CH3.2Sn/c1(3-7-13-9-5-11-15-13)2-4-8-14-10-6-12-16-14;;;;;;;;/h5-6,9-10H,1-4,7-8H2;6*1H3;;
• InChI Key: PGVIBGDMTHAVLY-UHFFFAOYSA-N
• Exact Mass: 576.01400
• Molecular Formula: C20H34S2Sn2
• Molecular Weight: 576.0
• SMILES: C[Sn](C)(C)C1=CC=C(S1)CCCCCCC2=CC=C(S2)[Sn](C)(C)C
• Topological: 56.5
• Monoisotopic Mass: 578.01460
• Synonyms: 1,6-Bis(5-(trimethylstannyl)thiophen-2-yl)hexane, 1884354-21-5, SCHEMBL19639707, G66276

Application

1,6-Bis(5-(trimethylstannyl)thiophen-2-yl)hexane is primarily used as a key precursor in the synthesis of conjugated polymers for organic electronics, such as organic photovoltaics (OPVs) and field-effect transistors (OFETs). Its bifunctional stannyl-thiophene structure enables efficient Stille coupling reactions, facilitating the construction of high-performance semiconducting materials. Researchers also employ this compound in the development of novel donor-acceptor copolymers for optoelectronic applications. Its stability and reactivity make it a valuable tool in exploratory materials chemistry.

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