Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H10NO3S.Na |
Molecular Weight | 271.267 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[O-]S(=O)(=O)C1=CC=C(NC2=CC=CC=C2)C=C1
InChI
InChIKey=DGXTZMPQSMIFEC-UHFFFAOYSA-M
InChI=1S/C12H11NO3S.Na/c14-17(15,16)12-8-6-11(7-9-12)13-10-4-2-1-3-5-10;/h1-9,13H,(H,14,15,16);/q;+1/p-1
Approval Year
PubMed
Title | Date | PubMed |
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In-situ spectroelectrochemical evidences for the copolymerization of o-toluidine with diphenylamine-4-sulphonic acid by UV-visible spectroscopy. | 2002 Jan 1 |
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[Study on the inclusion interaction of water-soluble p-(N,N-dimethylamino)-calix[8]arene with diphenylamine-4-sulfonic sodium salt]. | 2005 Apr |
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Structural and ionization effects on the adsorption behaviors of some anilinic compounds from aqueous solution onto high-area carbon-cloth. | 2005 Apr 11 |
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Facile synthesis and optimization of conductive copolymer nanoparticles and nanocomposite films from aniline with sulfodiphenylamine. | 2006 Feb 1 |
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Synthesis and characterization of processable multi-walled carbon nanotubes-sulfonated polydiphenylamine graft copolymers. | 2007 Oct |
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S-Benzyl-thiouronium 4-anilinobenzene-sulfonate. | 2008 Aug 30 |
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Quenching of the electrochemiluminescence of tris(2,2'-bipyridine)-ruthenium(II) by sodium diphenylamine-4-sulfonate. | 2009 Jun |
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Structure-based discovery of triphenylmethane derivatives as inhibitors of hepatitis C virus helicase. | 2009 May 14 |
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228-165-6
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DTXSID5064126
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6152-67-6
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3E2UX1382O
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148340
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517002
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m8693
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PRIMARY | Merck Index |
SUBSTANCE RECORD