Description

4-(2-Aminophenoxy)phthalonitrile (CAS No. 152633-90-4) is a high-purity organic compound with the molecular formula C₁₄H₉N₃O, widely used in advanced chemical research and material science applications. This compound, also known by its IUPAC name 4-(2-aminophenoxy)benzene-1,2-dicarbonitrile, features a unique aromatic structure combining an aminophenoxy group with a phthalonitrile core, making it a valuable precursor for synthesizing phthalocyanines and other nitrogen-containing heterocycles. Its high reactivity and stability under controlled conditions ensure consistent performance in polymerization, coordination chemistry, and optoelectronic material development. Ideal for researchers, this product is rigorously tested for purity and supplied with detailed analytical documentation, including HPLC, NMR, and MS data.

Properties

• CAS Number: 152633-90-4
• Complexity: 377
• IUPAC Name: 4-(2-aminophenoxy)phthalonitrile
• InChI: InChI=1S/C14H9N3O/c15-8-10-5-6-12(7-11(10)9-16)18-14-4-2-1-3-13(14)17/h1-7H,17H2
• InChI Key: LIBGSMDCGXNBAM-UHFFFAOYSA-N
• Exact Mass: 235.074561919
• Molecular Formula: C14H9N3O
• Molecular Weight: 235.24
• SMILES: C1=CC=C(C(=C1)N)OC2=CC(=C(C=C2)C#N)C#N
• Topological: 82.8
• Monoisotopic Mass: 235.074561919
• Synonyms: 4-(2-aminophenoxy)phthalonitrile, 4-(2-AMINOPHENOXY)-1,2-BENZENEDICARBONITRILE, 152633-90-4, SCHEMBL7115607, LIBGSMDCGXNBAM-UHFFFAOYSA-N, H27527

Application

4-(2-Aminophenoxy)phthalonitrile serves as a critical building block in the synthesis of phthalocyanine dyes and pigments, which are widely used in photodynamic therapy, organic semiconductors, and nonlinear optical materials. Its bifunctional structure enables crosslinking in high-performance polymers, enhancing thermal and mechanical properties. Researchers also utilize it to develop metal-organic frameworks (MOFs) and coordination complexes for catalytic and sensing applications.

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