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Catalog Number:
44230
CAS Number:
37882-75-0
Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
Purity:
≥ 93% (GC)
Documents
$73.21 /200MG
Pack Size Availability Price
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Product Information

Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde is a versatile compound recognized for its unique structural properties, making it an essential building block in organic synthesis and materials science. This compound features two aldehyde functional groups, which enhance its reactivity and allow for diverse applications in the development of organic semiconductors, particularly in the fabrication of organic photovoltaic devices and field-effect transistors. Its distinctive thieno[3,2-b]thiophene backbone contributes to its excellent electronic properties, enabling efficient charge transport and improved device performance.

Researchers and industry professionals can leverage Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde in the synthesis of novel conjugated polymers and small molecules for advanced electronic applications. Its ability to undergo various chemical modifications opens avenues for tailoring properties to meet specific application requirements. Additionally, this compound can serve as a precursor for the development of sensors and optoelectronic materials, showcasing its potential in cutting-edge technologies. With its unique features and practical applications, Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde stands out as a valuable asset in the field of organic electronics.

CAS Number
37882-75-0
Purity
≥ 93% (GC)
Molecular Formula
C8H4O2S2
Molecular Weight
196.24
MDL Number
MFCD03931117
PubChem ID
361865
Melting Point
274 °C (dec.)
Appearance
Orange to brown crystalline powder
Conditions
Store at 2 - 8 °C
General Information
CAS Number
37882-75-0
Purity
≥ 93% (GC)
Molecular Formula
C8H4O2S2
Molecular Weight
196.24
MDL Number
MFCD03931117
PubChem ID
361865
Melting Point
274 °C (dec.)
Appearance
Orange to brown crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde is widely utilized in research focused on:

  • Organic Electronics: This compound is a key building block in the synthesis of organic semiconductors, which are essential for fabricating organic light-emitting diodes (OLEDs) and organic solar cells, offering flexibility and lightweight properties compared to traditional materials.
  • Material Science: It is used in the development of advanced materials with unique electronic properties, making it suitable for applications in sensors and transistors, enhancing performance and efficiency in electronic devices.
  • Pharmaceutical Research: The compound serves as a precursor in the synthesis of various biologically active molecules, aiding in the discovery and development of new drugs with potential therapeutic effects.
  • Photovoltaic Applications: Its role in the creation of donor-acceptor systems in solar cells improves energy conversion efficiency, making renewable energy technologies more viable and sustainable.
  • Polymer Chemistry: It is incorporated into polymer matrices to enhance conductivity and stability, which is crucial for developing high-performance materials used in electronics and coatings.

Citations