Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H8O7S2 |
Molecular Weight | 304.296 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC2=C(C=C1)C=C(C=C2S(O)(=O)=O)S(O)(=O)=O
InChI
InChIKey=DOBIZWYVJFIYOV-UHFFFAOYSA-N
InChI=1S/C10H8O7S2/c11-7-2-1-6-3-8(18(12,13)14)5-10(9(6)4-7)19(15,16)17/h1-5,11H,(H,12,13,14)(H,15,16,17)
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity. | 1993 Jul 9 |
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The historical aspects of sunscreens. | 2001 Nov 15 |
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Investigation of naphtalene sulfonate compounds sorption in a soil artificially contaminated using batch and column assays. | 2002 |
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Excited state proton transfer in reverse micelles. | 2002 Jun 26 |
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Effect of pressure on the proton transfer rate from a photoacid to a solvent. 4. Photoacids in methanol. | 2005 Jun 2 |
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Temperature dependence of excited state proton transfer in ice. | 2007 Jun 14 |
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Temperature dependence of solvation dynamics of probe molecules in methanol-doped ice and in liquid ethanol. | 2007 Oct 25 |
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Ultra-fast and optimized method for the preparation of rodent testicular cells for flow cytometric analysis. | 2009 Mar 6 |
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m7743
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2073
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DTXSID3059470
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118-32-1
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204-245-6
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SUBSTANCE RECORD