(3,6-Dimethoxythieno[3,2-b]thiophene-2,5-diyl)bis(trimethylstannane)

98%

Reagent Code: #177590
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CAS Number 1801357-03-8

science Other reagents with same CAS 1801357-03-8

blur_circular Chemical Specifications

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Weight 525.89 g/mol
Formula C₁₄H₂₄O₂S₂Sn₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics. It enables the preparation of high-performance organic semiconductors used in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound’s stannane groups facilitate Stille coupling reactions, allowing efficient incorporation into complex polymer chains with good regioregularity and electronic properties. Its structure supports extended π-conjugation, enhancing charge carrier mobility in thin-film devices. Commonly employed in research and development of solution-processable electronic materials.

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inventory 250mg
10-20 days ฿13,780.00

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(3,6-Dimethoxythieno[3,2-b]thiophene-2,5-diyl)bis(trimethylstannane)
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Used as a key intermediate in the synthesis of conjugated polymers for organic electronics. It enables the preparation of high-performance organic semiconductors used in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound’s stannane groups facilitate Stille coupling reactions, allowing efficient incorporation into complex polymer chains with good regioregularity and electronic properties. Its structure supports extended π-conjugation, enhancing charge carrier mobility

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics. It enables the preparation of high-performance organic semiconductors used in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound’s stannane groups facilitate Stille coupling reactions, allowing efficient incorporation into complex polymer chains with good regioregularity and electronic properties. Its structure supports extended π-conjugation, enhancing charge carrier mobility in thin-film devices. Commonly employed in research and development of solution-processable electronic materials.

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