Description

Dibenzo[g,p]chrysen-2,3,6,7,10,11,14,15-octaol (CAS No. 1246204-19-2) is a high-purity polycyclic aromatic compound with the molecular formula C₂₆H₁₆O₈. This octaol derivative features a rigid, planar hexacyclic structure with eight hydroxyl groups, making it a valuable intermediate for advanced organic synthesis and materials science research. The compound’s extended π-conjugated system and multiple reactive sites enable its use in the development of organic semiconductors, luminescent materials, and supramolecular assemblies. Available as a fine powder with ≥95% purity (HPLC), it is supplied in amber glass vials under inert atmosphere to ensure stability. Researchers can leverage its unique electronic and steric properties for designing novel functional materials with tailored optoelectronic characteristics.

Properties

• CAS Number: 1246204-19-2
• Complexity: 643
• IUPAC Name: hexacyclo[12.12.0.02,7.08,13.015,20.021,26]hexacosa-1(14),2,4,6,8,10,12,15,17,19,21,23,25-tridecaene-4,5,10,11,17,18,23,24-octol
• InChI: InChI=1S/C26H16O8/c27-17-1-9-10-2-18(28)22(32)6-14(10)26-16-8-24(34)20(30)4-12(16)11-3-19(29)23(33)7-15(11)25(26)13(9)5-21(17)31/h1-8,27-34H
• InChI Key: LYEYINGUSZFQDC-UHFFFAOYSA-N
• Exact Mass: 456.08451746
• Molecular Formula: C26H16O8
• Molecular Weight: 456.4
• SMILES: C1=C2C3=CC(=C(C=C3C4=C(C2=CC(=C1O)O)C5=CC(=C(C=C5C6=CC(=C(C=C64)O)O)O)O)O)O
• Topological: 162
• Monoisotopic Mass: 456.08451746
• Synonyms: Dibenzo[g,p]chrysen-2,3,6,7,10,11,14,15-octaol, 1246204-19-2, YSWG473, SCHEMBL28907259, MFCD34473870, BS-46915, CS-0170642, F74470, dibenzo-[g,p]chrysene-2,3,6,7,10,11,14,15-octaol, Dibenzo[g,p]chrysene-2,3,6 ,7,10,11,14,15-octol, hexacyclo[12.12.0.02,7.08,13.015,20.021,26]hexacosa-1(14),2,4,6,8,10,12,15,17,19,21,23,25-tridecaene-4,5,10,11,17,18,23,24-octol

Application

Dibenzo[g,p]chrysen-2,3,6,7,10,11,14,15-octaol serves as a key building block for π-extended organic electronic materials due to its multi-hydroxyl functionalization and large aromatic surface area. The compound shows promise in the development of organic field-effect transistors (OFETs) and perovskite solar cells as a hole-transporting material. Its multiple redox-active sites make it suitable for investigating charge transport mechanisms in conjugated systems. Researchers also utilize this octaol derivative as a precursor for synthesizing graphene-like nanostructures through controlled oxidative coupling reactions.

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