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=C(C=C2C=C1)S(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 |
|---|---|---|
| Ultra-fast and optimized method for the preparation of rodent testicular cells for flow cytometric analysis. | 2009-03-06 |
|
| Temperature dependence of solvation dynamics of probe molecules in methanol-doped ice and in liquid ethanol. | 2007-10-25 |
|
| Temperature dependence of excited state proton transfer in ice. | 2007-06-14 |
|
| Effect of pressure on the proton transfer rate from a photoacid to a solvent. 4. Photoacids in methanol. | 2005-06-02 |
|
| Excited state proton transfer in reverse micelles. | 2002-06-26 |
|
| Investigation of naphtalene sulfonate compounds sorption in a soil artificially contaminated using batch and column assays. | 2002 |
|
| The historical aspects of sunscreens. | 2001-11-15 |
|
| Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity. | 1993-07-09 |
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m7743
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2073
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DTXSID3059470
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67041
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5995F5R8Y9
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118-32-1
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204-245-6
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SUBSTANCE RECORD
