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In1654, 1,3-Bis(2-Ethylhexyl)-5,7-Bis(5-(Trimethylstannyl)Thiophen-2-Yl)Benzo[1,2-C:4,5-C']Dithiophene-4,8-Dione CAS NO 2111948-40-2


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CAS No.:2111948-40-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

In1654, 1,3-Bis(2-Ethylhexyl)-5,7-Bis(5-(Trimethylstannyl)Thiophen-2-Yl)Benzo[1,2-C:4,5-C']Dithiophene-4,8-Dione is a high-purity, functionalized organic semiconductor building block designed for advanced materials research and development. This compound is critical for synthesizing next-generation conjugated polymers and small molecules with tailored electronic properties. It is primarily sought by R&D chemists and material scientists working in the fields of organic electronics and photovoltaics.

Application

  • Organic Photovoltaic (OPV) Cells: As a key electron-accepting or donor-acceptor building block in the synthesis of low-bandgap polymers for high-efficiency solar cells.
  • Organic Field-Effect Transistors (OFETs): Used to develop novel semiconducting materials for flexible and printed electronics.
  • Perovskite Solar Cells: Potential application as a hole-transporting material (HTM) or interfacial layer component to improve device stability and performance.
  • Organic Light-Emitting Diodes (OLEDs): Serves as a precursor for emissive or charge-transport layers in display and lighting technologies.
  • Chemical Synthesis & Material Science: A versatile intermediate for Stille cross-coupling reactions, enabling the construction of complex π-conjugated systems for fundamental research.
  • Photodetectors & Sensors: Development of sensitive organic-based detectors for specific wavelengths or chemical sensing applications.

Basic Information

Product Name In1654, 1,3-Bis(2-Ethylhexyl)-5,7-Bis(5-(Trimethylstannyl)Thiophen-2-Yl)Benzo[1,2-C:4,5-C']Dithiophene-4,8-Dione
CAS No. 2111948-40-2
Molecular Formula C52H70O2S4Sn2
Molecular Weight 1086.98 g/mol
Synonyms 1,3-Bis(2-ethylhexyl)-5,7-bis[5-(trimethylstannyl)-2-thienyl]benzo[1,2-c:4,5-c']dithiophene-4,8-dione; BDT-Tin monomer; Stannylated benzo[1,2-c:4,5-c']dithiophene-4,8-dione derivative; OPV monomer In1654; Tin-functionalized BDT donor unit; (5,7-Bis(5-(Trimethylstannyl)thiophen-2-yl)-1,3-bis(2-ethylhexyl)benzo[1,2-c:4,5-c']dithiophene-4,8-dione); Electron acceptor building block
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Quality Control

Every batch of In1654 is synthesized and purified under stringent conditions to ensure high chemical purity and optimal performance in sensitive coupling reactions. Our quality assurance includes comprehensive analytical characterization using techniques such as NMR, HPLC, and elemental analysis. A Certificate of Analysis (COA) detailing batch-specific purity, identity, and residual solvent levels is provided with each shipment to support your R&D and quality protocols.

Storage

Preserve in a tightly closed container, protected from light. For long-term stability, store the product in a freezer at -20°C to -10°C under an inert atmosphere (argon or nitrogen). Allow the sealed container to reach room temperature before opening to prevent moisture condensation. Keep away from strong oxidizing agents.

Specification

Item Specification
Appearance Dark red to purple solid
Identification (NMR) Conforms to structure
Purity (HPLC) ≥ 95% (Area %)
Tin Content Conforms to theoretical
Residual Solvents (GC) Meets ICH guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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