1,5-Dihydroxynaphthalene
1,5-Dihydroxynaphthalene structure
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Common Name | 1,5-Dihydroxynaphthalene | ||
|---|---|---|---|---|
| CAS Number | 83-56-7 | Molecular Weight | 160.169 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 375.4±15.0 °C at 760 mmHg | |
| Molecular Formula | C10H8O2 | Melting Point | 259-261ºC | |
| MSDS | Chinese USA | Flash Point | 193.5±15.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Effects of cyano-substituents on the molecular packing structures of conjugated polymers for bulk-heterojunction solar cells.
ACS Appl. Mater. Interfaces 6(18) , 15774-82, (2014) The molecular packing structures of two conjugated polymers based on alkoxy naphthalene, one with cyano-substituents and one without, have been investigated to determine the effects of electron-withdrawing cyano-groups on the performance of bulk-heterojunctio... |
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Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides.
J. Med. Chem. 49 , 1932-8, (2006) The antiproliferative activity of the 14 isomeric monoxylosylated dihydroxynaphthalenes has been tested in vitro toward normal HFL-1 and 3T3 A31 cells as well as transformed T24 and 3T3 SV40 cells. The antiproliferative effect toward HFL-1 cells was correlate... |
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Photooxidation of 1,5-dihydroxynaphthalene with iridium complexes as singlet oxygen sensitizers.
Photochem. Photobiol. Sci. 10(6) , 895-903, (2011) Photooxidation reactions of 1,5-dihydroxynaphthalene (DHN) have been carried out in the presence of cyclometalated neutral and cationic iridium (Ir) complexes 1-6 as singlet oxygen ((1)O(2)) sensitizers in order to investigate the (1)O(2) generation quantum y... |
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Flavonoids and related compounds as inhibition of arachidonic acid peroxidation.
Prostaglandins 20(4) , 627-39, (1980) Until now only few data have been reported on biochemically explicable pharmacological effects of flavonoid structures. When tested against arachidonic acid metabolism many flavonoids were found to be effective against the lipoxygenase and cyclo-oxygenase pat... |
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Visible light-harvesting perylenebisimide-fullerene (C60) dyads with bidirectional "ping-pong" energy transfer as triplet photosensitizers for photooxidation of 1,5-dihydroxynaphthalene.
Chem. Commun. (Camb.) 48(31) , 3751-3, (2012) Visible light-harvesting perylenebisimide (PBI)-C(60) dyads were prepared as organic triplet photosensitizers for photooxidation of 1,5-dihydroxynaphthalene and the efficiency of the dyads is 6-fold of the conventional Ir(III) complex triplet photosensitizer.... |
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Interactions of sulfhydryl agents and soybean lipoxygenase inhibitors.
Biochem. Pharmacol. 30(12) , 1677-84, (1981)
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Copper-induced peroxidation of phosphatidylserine-containing liposomes is inhibited by nanomolar concentrations of specific antioxidants.
Chem. Phys. Lipids 150(2) , 186-203, (2007) Copper-induced peroxidation of liposomal palmitoyllinoleoyl-phosphatidylcholine (PLPC) is inhibited by alpha-tocopherol at micromolar concentrations. In our previous study we found that when the liposomes contain phosphatidylserine (PS), nanomolar concentrati... |
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Electrolysis-mediated irreversible inactivation of lipoxygenase directed toward electroaffinity labelling.
Biochem. Biophys. Res. Commun. 123(1) , 156-62, (1984) Irreversible inhibition of soybean lipoxygenase-1 (SL-1) was accomplished via a controlled potential oxidative electrolysis of 1,5-dihydroxynaphthalene (1,5-DHN) at +0.8 V vs SCE. The inactivation of SL-1 with this known inhibitor was greatly enhanced under t... |