Description

1-Diazonio-6-nitro-4-sulfonaphthalen-2-olate (CAS: 63589-25-3) is a highly specialized diazonium compound with the molecular formula C₁₀H₅N₃O₆S. This chemical is designed for advanced research applications, offering exceptional reactivity due to its diazonio and nitro functional groups. It is widely utilized in organic synthesis, photochemistry, and materials science, where its unique structural properties enable precise molecular modifications. Available in high-purity grades, this product is ideal for researchers requiring consistent performance in sensitive experimental conditions. Proper handling under inert atmospheres is recommended due to its potential instability.

Properties

• CAS Number: 63589-25-3
• Complexity: 544
• IUPAC Name: 1-diazonio-6-nitro-4-sulfo-naphthalen-2-olate
• InChI: InChI=1S/C10H5N3O6S/c11-12-10-6-2-1-5(13(15)16)3-7(6)9(4-8(10)14)20(17,18)19/h1-4H,(H-,14,17,18,19)
• InChI Key: CCFWJWRQXDDAEJ-UHFFFAOYSA-N
• Exact Mass: 294.98990606
• Molecular Formula: C10H5N3O6S
• Molecular Weight: 295.23
• SMILES: C1=CC2=C(C(=CC(=C2C=C1[N+](=O)[O-])S(=O)(=O)O)[O-])[N+]#N
• Topological: 160
• Monoisotopic Mass: 294.98990606
• Synonyms: 63589-25-3, ARWGNJSGPHDIKK-UHFFFAOYSA-N, AKOS025310927, DB-054508, NS00054549, 4-Diazo-7-nitro-3-oxonaphthalene-1-sulfonic acid

This compound is primarily used as a photoresist component in microelectronics fabrication, leveraging its light-sensitive diazonium group. It also serves as a key intermediate in the synthesis of azo dyes and other chromophores for analytical chemistry applications. Researchers employ it in surface modification studies due to its ability to form covalent bonds with substrates under controlled conditions.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.