Weight | 456.5 g/mol |
---|---|
Formula | C34H16O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 9 |
Rotatable Bonds | 0 |
116-71-2 (116-71-2)
violanthrone · anthra(9,1,2-cde)benzo(rst)pentaphene-5,10-dione
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- New perylene and violanthrone dyestuffs for fluorescent collectors (Dyes and Pigments, 1989)
- On the Electrical Conductivity of Violanthrone, IsoViolanthrone, and Pyranthrone (Journal of Chemical Physics, 1950)
- Excitation of violanthrone by singlet oxygen. A chemiluminescence mechanism (The Journal of Physical Chemistry, 1968)
- Quinolin-65 and Violanthrone-79 as Model Molecules for the Kinetics of the Adsorption of C7 Athabasca Asphaltene on Macroporous Solid Surfaces (Energy & Fuels, 2006)
- A Breakthrough toward Long Wavelength Cationic Photopolymerization: Initiating Systems Based on Violanthrone Derivatives and Silyl Radicals (Macromolecules, 2011)
- Photoconductivity of Violanthrone (Journal of Chemical Physics, 1952)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - violanthrone
- anthra(9,1,2-cde)benzo(rst)pentaphene-5,10-dione
-
SMILESC1=CC=C2C(=C1)C3=C4C(=CC=C5C4=C(C=C3)C6=C7C5=CC=C8C7=C(C=C6)C9=CC=CC=C9C8=O)C2=O
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InChIKeyYKSGNOMLAIJTLT-UHFFFAOYSA-N
- Pubchem - 116-71-2
- Wikipedia - violanthrone
Violanthrone, also known as Dibenzanthrone, is an organic compound that serves as a vat dye and a precursor to other vat dyes. X-ray crystallography confirms that the molecule is planar with C2v symmetry. Isomeric with violanthrone is isoviolanthrone, which has a centrosymmetric structure.
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