Exploring the Chemical Properties of Dibromo-Thiophene Dicarboxylic Acid
Understanding the chemical nuances of organic intermediates is fundamental for successful synthesis and material design. 2,5-Dibromo-3,4-thiophenedicarboxylic acid (CAS: 190723-12-7) is a prime example of such a critical compound, offering a unique combination of functional groups that make it invaluable in advanced chemical synthesis, particularly for porous materials like MOFs and COFs.
As a leading supplier in China, we are dedicated to providing high-purity (97% min) 2,5-Dibromo-3,4-thiophenedicarboxylic acid. The molecular structure itself is key to its utility. It features a central thiophene ring, a five-membered aromatic heterocycle containing sulfur. This ring is substituted at the 2 and 5 positions with bromine atoms, and at the 3 and 4 positions with carboxylic acid (-COOH) groups. This specific arrangement imbues the molecule with distinct chemical properties essential for its role as a linker.
The presence of two bromine atoms on the thiophene ring offers several advantages. Bromine is an electron-withdrawing group, which can influence the electronic properties of the thiophene ring and, consequently, the final porous framework. More importantly, these bromine atoms serve as reactive sites for various organic transformations, including cross-coupling reactions such as Suzuki, Stille, or Sonogashira couplings. This allows for further functionalization of the linker, either before or after its incorporation into a MOF or COF structure, thereby tailoring the material's properties for specific applications like catalysis or sensing. Researchers looking to buy 2,5-dibromo-3,4-thiophenedicarboxylic acid are often interested in these post-synthetic modification capabilities.
The two carboxylic acid groups are the primary functional moieties responsible for coordinating with metal ions or clusters to form MOFs. These groups can deprotonate to form carboxylate anions, which readily chelate or bridge metal centers. The geometry and spacing of these carboxylic acid groups on the rigid thiophene core are crucial for dictating the topology and pore dimensions of the resulting MOF. This precise structural control is what makes high-purity linkers so vital. Our commitment as a manufacturer in China ensures you receive a product with consistent structural integrity.
When planning to buy high purity dibromothiophene dicarboxylic acid, consider the advantages its unique chemical structure offers. It provides rigidity and defined connectivity for building ordered porous networks. The combination of reactive halogens and coordinating carboxylates makes it an exceptionally versatile building block for advanced materials. For those engaged in custom synthesis, this compound is an excellent starting material for a wide array of organic transformations.
We are proud to be a reliable source for this important chemical intermediate. Our dedication to quality and our expertise in organic synthesis make us an ideal partner for your research and development needs. If you require 2,5-Dibromo-3,4-thiophenedicarboxylic acid for your next project, please reach out to us for a quotation and sample. Discover how the chemical properties of this compound can unlock new possibilities in material science.
Perspectives & Insights
Logic Thinker AI
“Researchers looking to buy 2,5-dibromo-3,4-thiophenedicarboxylic acid are often interested in these post-synthetic modification capabilities.”
Molecule Spark 2025
“The two carboxylic acid groups are the primary functional moieties responsible for coordinating with metal ions or clusters to form MOFs.”
Alpha Pioneer 01
“These groups can deprotonate to form carboxylate anions, which readily chelate or bridge metal centers.”