Description
2-Amino-[1,1′-biphenyl]-4,4′-dicarboxylic acid (CAS No. 1240557-01-0) is a high-purity biphenyl derivative extensively utilized in organic synthesis, pharmaceutical research, and material science applications. This compound features a molecular formula of C14H11NO4 and is characterized by its bifunctional carboxylic acid groups and an amino substituent, making it a versatile intermediate for coupling reactions, metal-organic frameworks (MOFs), and polymer synthesis. With a rigorous quality control process ensuring ≥95% purity (HPLC), this product is ideal for researchers requiring precise and reproducible results. Available in quantities ranging from milligrams to kilograms, it is packaged under inert conditions to guarantee stability and longevity. Store in a cool, dry place away from light and moisture to maintain optimal performance.
Properties
- CAS Number: 1240557-01-0
- Complexity: 349
- IUPAC Name: 3-amino-4-(4-carboxyphenyl)benzoic acid
- InChI: InChI=1S/C14H11NO4/c15-12-7-10(14(18)19)5-6-11(12)8-1-3-9(4-2-8)13(16)17/h1-7H,15H2,(H,16,17)(H,18,19)
- InChI Key: FYEKGZUXGKAJJQ-UHFFFAOYSA-N
- Exact Mass: 257.06880783
- Molecular Formula: C14H11NO4
- Molecular Weight: 257.24
- SMILES: C1=CC(=CC=C1C2=C(C=C(C=C2)C(=O)O)N)C(=O)O
- Topological: 101
- Monoisotopic Mass: 257.06880783
- Synonyms: 2-Amino-[1,1′-biphenyl]-4,4′-dicarboxylic acid, 1240557-01-0, MFCD32644766, YSZC118, SCHEMBL15901215, XH1521, 2-amino-4,4′-biphenyl dicarboxylic acid, 3-amino-4-(4-carboxyphenyl)benzoic acid, BS-51924, SY071057, CS-0110764, E77147, 10.14272/FYEKGZUXGKAJJQ-UHFFFAOYSA-N.1, doi:10.14272/FYEKGZUXGKAJJQ-UHFFFAOYSA-N.1, 2-Aminobiphenyl-4,4 inverted exclamation mark -dicarboxylic Acid
2-Amino-[1,1′-biphenyl]-4,4′-dicarboxylic acid serves as a critical building block in the synthesis of advanced materials, including luminescent polymers and porous coordination networks. Its bifunctional carboxyl groups enable efficient conjugation with metal ions for MOF construction, while the amino group facilitates further derivatization in drug discovery. Researchers also employ this compound in supramolecular chemistry for designing tailored molecular architectures. Its stability and reactivity make it a preferred choice for academic and industrial R&D.
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