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Atomfair 4-Aminophenyl 4-Aminobenzoate C13H12N2O2

Description 4-Aminophenyl 4-Aminobenzoate (CAS No. 20610-77-9) is a high-purity aromatic ester compound with the molecular formula C13H12N2O2. This bifunctional organic intermediate features two primary amine groups, making it a versatile building block for pharmaceutical synthesis, polymer modification, and advanced material research. The compound’s crystalline structure and defined purity (>98%) ensure reproducibility in sensitive applications. Available in gram to kilogram quantities, our product undergoes rigorous QC testing including HPLC, NMR, and mass spectrometry to guarantee batch-to-batch consistency. Ideal for researchers developing photoactive materials, liquid crystal polymers, or covalent organic frameworks (COFs) due to its conjugated aromatic system and reactive amine termini.

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Description

Description

4-Aminophenyl 4-Aminobenzoate (CAS No. 20610-77-9) is a high-purity aromatic ester compound with the molecular formula C13H12N2O2. This bifunctional organic intermediate features two primary amine groups, making it a versatile building block for pharmaceutical synthesis, polymer modification, and advanced material research. The compound’s crystalline structure and defined purity (>98%) ensure reproducibility in sensitive applications. Available in gram to kilogram quantities, our product undergoes rigorous QC testing including HPLC, NMR, and mass spectrometry to guarantee batch-to-batch consistency. Ideal for researchers developing photoactive materials, liquid crystal polymers, or covalent organic frameworks (COFs) due to its conjugated aromatic system and reactive amine termini.

  • CAS No: 20610-77-9
  • Molecular Formula: C13H12N2O2
  • Molecular Weight: 228.25
  • Exact Mass: 228.089877630
  • Monoisotopic Mass: 228.089877630
  • IUPAC Name: (4-aminophenyl) 4-aminobenzoate
  • SMILES: C1=CC(=CC=C1C(=O)OC2=CC=C(C=C2)N)N
  • Synonyms: 4-Aminophenyl 4-aminobenzoate, 20610-77-9, DTXSID50573274, DTXCID70524046, 810-934-8

Application

This bifunctional monomer serves as a key intermediate in synthesizing polyimide precursors for high-temperature polymers. Researchers utilize its amine groups for covalent attachment in surface modification of medical devices. The compound’s UV-absorbing properties make it valuable in developing light-stabilizing additives for specialty coatings. Pharmaceutical chemists employ it as a scaffold for novel drug candidates targeting inflammatory pathways.

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