Cas no 88460-78-0 (2-Furancarboxylic acid,5-(2-carboxyphenyl)-)

2-Furancarboxylic acid,5-(2-carboxyphenyl)- is a bifunctional organic compound featuring both furan and benzoic acid moieties. This structure imparts unique reactivity, making it valuable as an intermediate in organic synthesis, particularly for constructing heterocyclic frameworks. The presence of two carboxyl groups enhances its versatility in coupling reactions, esterifications, and metal coordination chemistry. Its aromatic furan ring contributes to electron-rich characteristics, facilitating participation in cycloadditions and electrophilic substitutions. The compound is commonly utilized in pharmaceutical and agrochemical research for developing bioactive molecules. Its dual functional groups allow for selective modifications, enabling tailored applications in material science and fine chemical production. Proper handling is advised due to potential sensitivity to heat and strong oxidizers.
2-Furancarboxylic acid,5-(2-carboxyphenyl)- structure
88460-78-0 structure
Product Name:2-Furancarboxylic acid,5-(2-carboxyphenyl)-
CAS No:88460-78-0
MF:C12H8O5
MW:232.188923835754
CID:709485
PubChem ID:7174478
Update Time:2025-10-30

2-Furancarboxylic acid,5-(2-carboxyphenyl)- Chemical and Physical Properties

Names and Identifiers

    • 2-Furancarboxylic acid,5-(2-carboxyphenyl)-
    • 5-(2-Carboxy-phenyl)-furan-2-carboxylic acid
    • 5-(2-Carboxyphenyl)-furan-2-carboxylic acid
    • 5-(2-carboxyphenyl)furan-2-carboxylic acid
    • BB 0259504
    • BDBM50175435
    • DTXSID00428321
    • 5-(2-carboxyphenyl)furan-2-carboxylicAcid
    • CHEMBL197760
    • 88460-78-0
    • MDL: MFCD06739574
    • Inchi: 1S/C12H8O5/c13-11(14)8-4-2-1-3-7(8)9-5-6-10(17-9)12(15)16/h1-6H,(H,13,14)(H,15,16)
    • InChI Key: WMUYPMCIAJSRIN-UHFFFAOYSA-N
    • SMILES: O1C(C(=O)O)=CC=C1C1C=CC=CC=1C(=O)O

Computed Properties

  • Exact Mass: 232.03717335g/mol
  • Monoisotopic Mass: 232.03717335g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 3
  • Complexity: 314
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2
  • Topological Polar Surface Area: 87.7?2

2-Furancarboxylic acid,5-(2-carboxyphenyl)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Chemenu
CM527379-1g
5-(2-Carboxyphenyl)furan-2-carboxylic acid
88460-78-0 97%
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$577 2023-02-01
Crysdot LLC
CD11033925-1g
5-(2-Carboxyphenyl)furan-2-carboxylic acid
88460-78-0 97%
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Additional information on 2-Furancarboxylic acid,5-(2-carboxyphenyl)-

Comprehensive Analysis of 2-Furancarboxylic acid,5-(2-carboxyphenyl)- (CAS No. 88460-78-0): Properties, Applications, and Industry Trends

2-Furancarboxylic acid,5-(2-carboxyphenyl)-, identified by its CAS No. 88460-78-0, is a specialized organic compound with a unique molecular structure combining furan and benzoic acid moieties. This bifunctional molecule has garnered significant attention in pharmaceutical, agrochemical, and material science research due to its versatile reactivity. The compound's dual carboxyl groups enable diverse derivatization pathways, making it a valuable intermediate for synthesizing complex molecules.

Recent advancements in green chemistry have highlighted the potential of furan-based compounds like 5-(2-carboxyphenyl)-2-furancarboxylic acid as sustainable alternatives to petroleum-derived chemicals. With growing interest in bio-based materials, researchers are exploring its applications in polymer modification and biodegradable plastics. The compound's aromaticity and hydrogen-bonding capacity contribute to interesting photophysical properties, relevant for developing organic electronic materials.

The synthesis of CAS 88460-78-0 typically involves multi-step organic reactions, with careful control of reaction conditions to optimize yield and purity. Analytical characterization using HPLC-MS and NMR spectroscopy confirms its structural integrity. In pharmaceutical applications, its framework serves as a precursor for heterocyclic drug development, particularly in designing molecules with improved bioavailability and target specificity.

Market trends indicate rising demand for specialty carboxylic acids like this compound, driven by innovations in drug delivery systems and functional materials. Regulatory considerations emphasize proper handling procedures, though it doesn't fall under restricted categories. Storage recommendations include protection from moisture and extreme temperatures to maintain stability.

Ongoing research explores novel derivatives of 2-Furancarboxylic acid,5-(2-carboxyphenyl)- for catalysis applications and coordination chemistry. Its metal-chelating properties show promise in developing new ligand systems for transition metal complexes. The compound's environmental fate and ecotoxicological profile are subjects of current investigation to ensure sustainable use across industries.

Quality control protocols for CAS No. 88460-78-0 typically involve chromatographic purity assessment and spectroscopic verification. Suppliers often provide technical specifications including minimum purity levels (usually ≥95%) and appropriate analytical certificates. The compound's structure-activity relationships continue to be studied for rational design of more efficient chemical entities in various applications.

From a commercial perspective, 5-(2-carboxyphenyl)furan-2-carboxylic acid remains a niche product with specialized suppliers catering to research institutions and industrial laboratories. Pricing reflects the complexity of its synthesis and purification processes. Recent patent literature reveals growing intellectual property activity surrounding its derivatives, particularly in medicinal chemistry and material science applications.

The future outlook for this compound appears promising as interdisciplinary research uncovers new potential uses. Its combination of aromatic systems and functional groups positions it as a valuable building block in molecular design. As analytical techniques advance, deeper understanding of its physicochemical properties will likely reveal additional applications in emerging technological fields.

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