Results 101 to 110 of about 4,004 (121)
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Methylation of 3-methylxanthine with methyl benzenesulfonate

Pharmaceutical Chemistry Journal, 1967
In the preparation of theobromine from 3-methylxanthine, methyl benzenesulfonate has been used as the methylating agent.
V. M. Nesterov, I. E. Chubova
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ChemInform Abstract: PHOTOCHEMICAL REARRANGEMENT OF PHENYL BENZENESULFONATES

Chemischer Informationsdienst, 1978
AbstractDie Photoumlagerung des Sulfonats (Ia) ergibt die Produkte (II) und (IIIa) sowie das Phenol (IVa).
Y. OGATA, K. TAKAGI, S. YAMADA
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ChemInform Abstract: Direct Polyiodination of Benzenesulfonic Acid.

ChemInform, 1992
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
D. L. MATTERN, X. CHEN
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4-(4-Hydroxy-3,5-dimethylphenylazo)benzenesulfonic Acid

Acta Crystallographica Section C Crystal Structure Communications, 1995
In the solid state, the title compound, C 14 H 14 N 2 O 4 S.-H 2 O, exists as two forms: cubes (I) and needles (II). Both kinds of crystal are monohydrates. The dye molecules have the same geometry and are bonded by O-H...O intermolecular hydrogen bonds in both forms: an N + -H...O - intermolecular hydrogen bond in (II) and an N + -H...(O) 2 ...
N. Ehlinger, M. Perrin
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Do enantiomers of benzenesulfonic acid exist? Electron diffraction and quantum chemical study of molecular structure of benzenesulfonic acid

Journal of Molecular Structure, 2012
Abstract Molecular structure of benzenesulfonic acid was studied by gas-phase electron diffraction and quantum chemical (B3LYP/cc-pVTZ, МР2/cc-pVDZ, МР2/cc-pVTZ) methods. On the base of mass spectrometric analysis it was found that saturated vapor at Т = 396(9) K is represented by only molecular species, monomeric benzenesulfonic acid.
Nina I. Giricheva   +5 more
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Benzenesulfonic Acid, 2-Nitro-, (1-Methylethylidene)hydrazide

2008
[6655-27-2] C9H11N3O4S (MW 257.27) InChI = 1S/C9H11N3O4S/c1-7(2)10-11-17(15,16)9-6-4-3-5-8(9)12(13)14/h3-6,11H,1-2H3 InChIKey = SBNYNTYNEJTMQO-UHFFFAOYSA-N (a reagent used for synthesis of allenes from propargylic alcohols, for the reductive transposition of allylic alcohols and allylic bromides, and for the deoxygenation of ...
Mohammad Movassaghi, Omar K. Ahmad
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Direct polyiodination of benzenesulfonic acid

The Journal of Organic Chemistry, 1991
Daniell Lewis Mattern, Xinhua Chen
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The Ethanolysis of Allyl Benzenesulfonate

Journal of the American Chemical Society, 1952
Clarence G. Bergstrom, Samuel Siegel
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Benzenesulfonic Anhydride

2001
Raj K. Raheja, Carl R. Johnson
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