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D115606

Sigma-Aldrich

1,5-Dihydroxynaphthalene

97%

Synonym(s):

1,5-Naphthalenediol

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About This Item

Linear Formula:
C10H6(OH)2
CAS Number:
83-56-7
Molecular Weight:
160.17
Beilstein/REAXYS Number:
2044951
EC Number:
201-487-4
MDL number:
MFCD00003980
UNSPSC Code:
12352100
PubChem Substance ID:
24893367
NACRES:
NA.22

assay

97%

form

powder

mp

259-261 °C (dec.) (lit.)

SMILES string

Oc1cccc2c(O)cccc12

InChI

1S/C10H8O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1-6,11-12H

InChI key

BOKGTLAJQHTOKE-UHFFFAOYSA-N

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GHS07,GHS09

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Warning

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1B

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

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T J Holmes et al.
Biochemical and biophysical research communications, 123(1), 156-162 (1984-08-30)
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 these electrolytic conditions to which the
Yifan Liu et al.
Chemical communications (Cambridge, England), 48(31), 3751-3753 (2012-03-09)
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.
Interactions of sulfhydryl agents and soybean lipoxygenase inhibitors.
I Knippel et al.
Biochemical pharmacology, 30(12), 1677-1684 (1981-06-15)
J Baumann et al.
Prostaglandins, 20(4), 627-639 (1980-10-01)
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 pathways. Some flavonoids were predominant inhibitors
Shin-ya Takizawa et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 10(6), 895-903 (2011-02-08)
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 yield and photosensitizing durability of the
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