| Weight | 160.172 g/mol |
|---|---|
| Formula | C10H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
naphthalene-1,5-diol (83-56-7)
1,5-dihydroxynaphthalene
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- Photooxidation of 1,5-dihydroxynaphthalene with iridium complexes as singlet oxygen sensitizers (Photochemical and Photobiological Sciences, 2011)
- A Polymolecular DonorAcceptor Stack Made of Paraquat and a 1, 5-Dihydroxynaphthalene- Derived Crown Ether (Angewandte Chemie, 1989)
- Visible-light harvesting iridium complexes as singlet oxygen sensitizers for photooxidation of 1,5-dihydroxynaphthalene (Chemical Communications, 2012)
- Visible light-harvesting perylenebisimidefullerene (C60) dyads with bidirectional ping-pong energy transfer as triplet photosensitizers for photooxidation of 1,5-dihydroxynaphthalene (Chemical Communications, 2012)
- Electrosynthesis of highly conducting poly(1,5-dihydroxynaphthalene) in BF3.Et2O (European Polymer Journal, 2009)
- 1,8Bis(dimethylamino)4,5dihydroxynaphthalene, a Natural, Intramolecularly Protonated Proton Sponge with Zwitterionic Structure (Angewandte Chemie, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,5-dihydroxynaphthalene
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SMILESC1=CC2=C(C=CC=C2O)C(=C1)O
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InChIKeyBOKGTLAJQHTOKE-UHFFFAOYSA-N
- Pubchem - naphthalene-1,5-diol
- Wikipedia - 1,5-naphthalenediol
1,5-Dihydroxynaphthalene is an organic compound with the formula C10H6(OH)2. It is one of several isomers of dihydroxynaphthalene. It exists as colorless crystals that are soluble in polar organic solvents.
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naphthalene-1,5-diol
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