Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H8O2 |
Molecular Weight | 160.1693 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC2=C(C=C1)C=CC(O)=C2
InChI
InChIKey=DFQICHCWIIJABH-UHFFFAOYSA-N
InChI=1S/C10H8O2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h1-6,11-12H
Molecular Formula | C10H8O2 |
Molecular Weight | 160.1693 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Covalent titanium aryldioxy one-, two-, and three-dimensional networks and their examination as Ziegler-Natta catalysts. | 2001 Apr 23 |
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X-ray structure of beta-cyclodextrin-2,7-dihydroxy-naphthalene.4.6 H(2)O: an unusually distorted macrocycle. | 2001 Jul 12 |
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Selective nonpeptidic inhibitors of herpes simplex virus type 1 and human cytomegalovirus proteases. | 2001 Mar |
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Synthesis of 3,5- and 3,6-linked calix[n]naphthalenes. | 2002 Feb 8 |
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UV-vis, IR and 1H NMR spectroscopic studies of some mono- and bis-azo-compounds based on 2,7-dihydroxynaphthalene and aniline derivatives. | 2005 Dec |
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Mechanism of cytotoxicity of catechols and a naphthalenediol in PC12-AC cells: the connection between extracellular autoxidation and molecular electronic structure. | 2005 Feb 1 |
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Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products. | 2005 Jun 16 |
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Naphthalene-2,3-diol-imidazole (1/1). | 2008 Aug 13 |
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A new route to obtain high-yield multiple-shaped gold nanoparticles in aqueous solution using microwave irradiation. | 2008 Jul 21 |
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Influence of the polymer backbone structure on the properties of aromatic ionomers with pendant sulfobenzoyl side chains for use as proton-exchange membranes. | 2010 Dec |
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Monoclinic CuO nanoflowers on resin support: recyclable catalyst to obtain perylene compound. | 2010 Dec 14 |
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2,7-Bis(prop-2-yn-1-yl-oxy)naphthalene. | 2010 Jun 9 |
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A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene 3-dimethylallyl-transferase reaction. | 2010 May 28 |
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Photoinduced formation of shape-selective Pt nanoparticles. | 2010 May 4 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:05:06 GMT 2023
by
admin
on
Fri Dec 15 19:05:06 GMT 2023
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Record UNII |
0TO8E448UD
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Record Status |
Validated (UNII)
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Record Version |
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209-478-7
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DTXSID2060387
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407541
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11397
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582-17-2
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0TO8E448UD
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C107946
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