(Sulfonylbis(Methylene))Dibenzene 二苄基砜
CAS 620-32-6 MFCD00022036
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- {SNA} B, Bioactive Small Molecules, Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfones, Sulfur Compounds, 细胞生物学
- {SNA} Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfones, Sulfur Compounds
- {SNA} B, Bioactive Small Molecules, Building Blocks, Cell Biology, Chemical Synthesis, Organic Building Blocks, Sulfones, Sulfur Compounds
- {uni_hamburg} no charge; carbocycle; aromatic; 6RingOnly; 6ring; sulfone; 1fragment
相关文献及参考
- Short: III/35E Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Oxygen-17 Author: Duddeck, H.; Toth, G.; Simon, A. Editor: Gupta, R.R.; Lechner, M.D. Source: Landolt-Börnstein, New Series Volume: III/35E Year: 2002 Keyword: Alipathic and Aromatic hydrocarbons; Coupling constant j; Nuclear Magnetic Resonance; chemical shifts δ ISBN: 3-540-42501-2 ISBN: 978-3-540-42501-4 Internet Resource: DOI:10.1007/b92953 RefComment: VII, 230 pages. With CD-ROM., Hardcover Abstract: This volume provides a comprehensive and evaluated compilation of nuclear magnetic resonance data. Chemical shifts and coupling constants of boron-11 and phosphorus-31 (subvol. A), fluorine-19 and nitrogen-15 (subvol. B), hydrogen-1 (subvol. C), carbon-13 (subvol. D), and oxygen-17 (subvol. E) compounds are tabulated together with the gross- and structure formulas and the most readily available solvents. Due to the large amount of the data merely chemical shifts are presented in the printed versions, and all the data, chemical shifts and coupling constants are provided on CD-ROM's.
- Short: EINECS Title: EINECS (European Inventory of Existing Commercial Chemical Substances) Source: Official Journal of the European Communities Volume: C 146 A (15.06.1990) Page: 1 Year: 1990 Internet Resource: http://ecb.jrc.ec.europa.eu/esis/index.php?PGM=ein Publish_Date: 1990/06/15
- Converted by strong bases e.g. NaNH2, n-BuLi or RMgX to its dimetallated derivative, which can, be e.g. monobenzylated: J. Am. Chem. Soc., 81, 1154 (1959), or dibenzylated: J. Am. Chem. Soc., 79, 6342 (1957) with benzyl chloride, and forms a monoadduct with benzophenone: J. Am. Chem. Soc., 89, 4566 (1967).
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