Cas no 1261978-66-8 (3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid)

3-(2-Carboxy-5-chlorophenyl)-4-fluorobenzoic acid is a bifunctional aromatic carboxylic acid derivative featuring both a chloro and a fluoro substituent, enhancing its reactivity and selectivity in synthetic applications. The presence of two carboxyl groups allows for versatile derivatization, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The electron-withdrawing effects of the chloro and fluoro substituents contribute to its stability and influence its participation in cross-coupling and condensation reactions. This compound is particularly useful in the preparation of complex heterocycles and active pharmaceutical ingredients (APIs), where precise functional group manipulation is required. Its high purity and well-defined structure ensure consistent performance in research and industrial processes.
3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid structure
1261978-66-8 structure
Product Name:3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid
CAS No:1261978-66-8
MF:C14H8ClFO4
MW:294.662326812744
MDL:MFCD18321541
CID:1223322
PubChem ID:53227414
Update Time:2025-10-27

3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid
    • 2-(5-CARBOXY-2-FLUOROPHENYL)-4-CHLOROBENZOIC ACID
    • DTXSID50690970
    • 1261978-66-8
    • 2-(5-Carboxy-2-fluorophenyl)-4-chlorobenzoic acid, 95%
    • 5-Chloro-6'-fluoro[1,1'-biphenyl]-2,3'-dicarboxylic acid
    • MFCD18321541
    • MDL: MFCD18321541
    • Inchi: 1S/C14H8ClFO4/c15-8-2-3-9(14(19)20)10(6-8)11-5-7(13(17)18)1-4-12(11)16/h1-6H,(H,17,18)(H,19,20)
    • InChI Key: OUVUPHHHSFNXSQ-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(C(=O)O)=C(C=1)C1C(=CC=C(C(=O)O)C=1)F

Computed Properties

  • Exact Mass: 294.0095146g/mol
  • Monoisotopic Mass: 294.0095146g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 3
  • Complexity: 389
  • 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: 3.3
  • Topological Polar Surface Area: 74.6?2

3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB328769-5 g
2-(5-Carboxy-2-fluorophenyl)-4-chlorobenzoic acid, 95%; .
1261978-66-8 95%
5g
€1159.00 2023-04-26
abcr
AB328769-5g
2-(5-Carboxy-2-fluorophenyl)-4-chlorobenzoic acid, 95%; .
1261978-66-8 95%
5g
€1159.00 2025-02-14

3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid Related Literature

Additional information on 3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid

Comprehensive Overview of 3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid (CAS No. 1261978-66-8)

3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid (CAS No. 1261978-66-8) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This fluorinated benzoic acid derivative is characterized by its unique molecular structure, which includes a carboxy group and a chlorophenyl moiety. Its chemical properties make it a valuable intermediate in the synthesis of more complex molecules, particularly in the development of bioactive compounds and drug candidates.

In recent years, the demand for fluorinated aromatic compounds like 3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid has surged due to their applications in medicinal chemistry. Researchers are particularly interested in its potential role as a building block for small-molecule inhibitors and therapeutic agents. The presence of both fluorine and chlorine atoms in its structure enhances its reactivity and binding affinity, making it a promising candidate for targeting specific enzyme pathways.

One of the most frequently asked questions about this compound revolves around its synthetic routes and purification methods. Laboratories often employ high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy to ensure its purity and structural integrity. Additionally, its solubility in polar solvents like dimethyl sulfoxide (DMSO) and methanol makes it versatile for various experimental setups.

The compound's relevance extends to green chemistry initiatives, where researchers explore eco-friendly synthesis methods to reduce waste and energy consumption. This aligns with the growing trend of sustainable chemical production, a topic highly searched in academic and industrial circles. Moreover, its potential applications in cancer research and neurodegenerative disease studies have sparked discussions in online forums and scientific communities.

From a commercial perspective, 3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid is often listed in chemical catalogs under its CAS number (1261978-66-8), making it easily identifiable for procurement. Suppliers typically highlight its high purity grade (>98%) and compliance with Good Manufacturing Practices (GMP), which are critical for pharmaceutical applications. The compound's stability under standard storage conditions (room temperature, dry environment) further adds to its practicality.

In summary, 3-(2-carboxy-5-chlorophenyl)-4-fluorobenzoic Acid (CAS No. 1261978-66-8) represents a compelling case study in modern chemical innovation. Its multifaceted applications, from drug discovery to material science, underscore its importance in advancing scientific and industrial progress. As research continues to uncover new uses for this compound, its prominence in the global chemical market is expected to grow.

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