Description

1,5-Bis(cyclohexylamino)anthracene-9,10-dione (CAS No. 15958-68-6) is a high-purity anthraquinone derivative with the molecular formula C₂₆H₃₀N₂O₂. This compound features two cyclohexylamino substituents at the 1,5-positions of the anthracenedione core, making it a valuable intermediate for organic synthesis and material science applications. It is supplied as a fine powder with ≥95% purity (HPLC) and is rigorously tested for consistency, ensuring optimal performance in research and industrial processes. Ideal for use in dye synthesis, photochemical studies, and as a functional building block for advanced materials. Store in a cool, dry place away from light and moisture to maintain stability.

Properties

• CAS Number: 15958-68-6
• Complexity: 569
• IUPAC Name: 1,5-bis(cyclohexylamino)anthracene-9,10-dione
• InChI: InChI=1S/C26H30N2O2/c29-25-20-14-8-16-22(28-18-11-5-2-6-12-18)24(20)26(30)19-13-7-15-21(23(19)25)27-17-9-3-1-4-10-17/h7-8,13-18,27-28H,1-6,9-12H2
• InChI Key: QSNJWMJODWUDPJ-UHFFFAOYSA-N
• Exact Mass: 402.230728204
• Molecular Formula: C26H30N2O2
• Molecular Weight: 402.5
• SMILES: C1CCC(CC1)NC2=CC=CC3=C2C(=O)C4=C(C3=O)C(=CC=C4)NC5CCCCC5
• Topological: 58.2
• Monoisotopic Mass: 402.230728204
• Synonyms: 15958-68-6, 1,5-DICYCLOHEXYLAMINOANTHRAQUINONE, 9,10-Anthracenedione, 1,5-bis(cyclohexylamino)-, 1,5-Bis(cyclohexylamino)-9,10-anthracenedione, Q8A8PS96FR, EINECS 240-093-7, DTXSID6065979, 1,5-Di(cyclohexylamino)anthracene-9,10-dione, 1,5-bis(cyclohexylamino)anthra-9,10-quinone, DTXCID8035138, 240-093-7, 1,5-bis(cyclohexylamino)anthracene-9,10-dione, 1,5-Bis(cyclohexylamino)anthraquinone, UNII-Q8A8PS96FR, SCHEMBL124713, QSNJWMJODWUDPJ-UHFFFAOYSA-N, MFCD00346383, STK874275, AKOS001600406, AS-15403, NS00025195, A906463, 1,5-bis(cyclohexylamino)-9,10-dihydroanthracene-9,10-dione

Application

1,5-Bis(cyclohexylamino)anthracene-9,10-dione is widely used as a key intermediate in the synthesis of anthraquinone-based dyes and pigments. Its unique structure lends itself to applications in photodynamic therapy research due to its potential light-absorbing properties. Researchers also utilize this compound in the development of organic semiconductors and conductive polymers for electronic devices.

Safety and Hazards

GHS Hazard Statements

• Not Classified
• Reported as not meeting GHS hazard criteria by 32 of 34 companies (only 5.9% companies provided GHS information). For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

• Not Classified

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