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CAS 10142-57-1

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Dinaphth[2,3-a:2′,3′-h]acridine-5,9,14,15,18(6H)-pentone

Description:
Dinaphth[2,3-a:2′,3′-h]acridine-5,9,14,15,18(6H)-pentone, with CAS number 10142-57-1, is a polycyclic aromatic compound characterized by its complex fused ring structure, which includes multiple naphthalene and acridine units. This compound typically exhibits a high degree of stability due to its extensive conjugated system, which can contribute to its electronic properties, such as fluorescence and absorption characteristics. It is generally insoluble in water but may dissolve in organic solvents, reflecting its hydrophobic nature. The presence of multiple carbonyl groups in its structure can influence its reactivity, making it a potential candidate for various chemical reactions, including oxidation and reduction processes. Additionally, compounds of this type may exhibit interesting photophysical properties, making them relevant in fields such as organic electronics, photonics, and materials science. However, specific applications and biological activities would depend on further research and characterization.
Formula:C29H13NO5
InChI:InChI=1S/C29H13NO5/c31-25-13-5-1-3-7-15(13)27(33)21-17(25)11-12-20-23(21)29(35)19-10-9-18-22(24(19)30-20)28(34)16-8-4-2-6-14(16)26(18)32/h1-12H,(H,30,35)
InChI key:InChIKey=HKFPGMSIDNGXLV-UHFFFAOYSA-N
SMILES:O=C1C2=C3C(C(=O)C4=C(N3)C=CC5=C4C(=O)C=6C(C5=O)=CC=CC6)=CC=C2C(=O)C=7C1=CC=CC7
Synonyms:
  • Dinaphth[2,3-a:2′,3′-h]acridan-5,9,14,15,18-pentone
  • Indanthren Orange F 3R
  • Carbanthrene Orange F 3R
  • C.I. 69540
  • Dinaphth[2,3-a:2′,3′-h]acridine-5,9,14,15,18(6H)-pentone
  • Vat Orange G
  • 6H-dinaphth[2,3-a,2',3'-h]acridine-5,9,14,15,18-pentaone
  • C.I.Vat Orange 16:C.I.69540
  • Dinaphth[2, 3-α: 2', 3'-h]acridine-5, 9, 14, 15, 18(6H)-pentone
  • Indanthren Orange F3R.
  • See more synonyms
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