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Catalog Number:
45020
CAS Number:
1015423-45-6
2,5-Dibromo-3,4-thiophenedicarboxylic anhydride
Purity:
≥ 98% (GC)
Synonym(s):
4,6-Dibromothieno[3,4-c]furan-1,3-dione
Documents
$525.09 /250MG
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Product Information

2,5-Dibromo-3,4-thiophenedicarboxylic anhydride is a versatile compound known for its unique chemical structure and properties, making it an essential material in various applications. This compound exhibits excellent reactivity, particularly in organic synthesis, where it serves as a key intermediate in the production of functionalized thiophene derivatives. Its bromine substituents enhance its electrophilic character, allowing for efficient coupling reactions, which are invaluable in the development of advanced materials, including organic semiconductors and photovoltaic devices.

Moreover, 2,5-Dibromo-3,4-thiophenedicarboxylic anhydride is increasingly utilized in the field of polymer chemistry, where it contributes to the synthesis of high-performance polymers with tailored electronic properties. Researchers appreciate its ability to facilitate the formation of complex molecular architectures, which can lead to innovative solutions in electronic and optoelectronic applications. With its robust performance and adaptability, this compound stands out as a crucial building block for professionals seeking to enhance their research and product development efforts.

Synonyms
4,6-Dibromothieno[3,4-c]furan-1,3-dione
CAS Number
1015423-45-6
Purity
≥ 98% (GC)
Molecular Formula
C6Br2O3S
Molecular Weight
311.93
MDL Number
MFCD27923031
PubChem ID
71721475
Appearance
Light yellow to brown to dark green powder to crystal
Conditions
Store at RT
General Information
Synonyms
4,6-Dibromothieno[3,4-c]furan-1,3-dione
CAS Number
1015423-45-6
Purity
≥ 98% (GC)
Molecular Formula
C6Br2O3S
Molecular Weight
311.93
MDL Number
MFCD27923031
PubChem ID
71721475
Appearance
Light yellow to brown to dark green powder to crystal
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,5-Dibromo-3,4-thiophenedicarboxylic anhydride is widely utilized in research focused on:

  • Organic Electronics: This compound serves as a key building block in the synthesis of organic semiconductors, which are essential for developing flexible electronics and organic photovoltaic cells.
  • Polymer Chemistry: It is used to create functionalized polymers that exhibit enhanced thermal and electrical properties, making it valuable in the production of advanced materials for coatings and adhesives.
  • Pharmaceutical Development: The compound plays a role in the synthesis of bioactive molecules, contributing to drug discovery processes, particularly in developing new therapeutic agents.
  • Environmental Applications: Its derivatives are explored for use in sensors and materials that can detect and remediate environmental pollutants, addressing critical challenges in environmental science.
  • Research in Material Science: The compound is studied for its potential in creating novel materials with unique optical and electronic properties, which can lead to innovations in various high-tech applications.

Citations