Difference between revisions of "Substance:Benzil"

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*Solubility properties: Not available
 
*Solubility properties: Not available
 
*Safety sheet: [http://msds.chem.ox.ac.uk/BE/benzil.html From Oxford University]
 
*Safety sheet: [http://msds.chem.ox.ac.uk/BE/benzil.html From Oxford University]
*Spectra: [http://webbook.nist.gov/cgi/cbook.cgi?ID=C134816&Units=SI&Type=IR-SPEC&Index=1#IR-SPEC IR], <sup>1</sup>H NMR, [http://www.ebi.ac.uk/nmrshiftdb/portal/js_pane/P-Results/nmrshiftdbaction/showDetailsFromHome/molNumber/10005895 <sup>13</sup>C NMR], MS.  Also check on [http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng SDBS].
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*Spectra: [http://webbook.nist.gov/cgi/cbook.cgi?ID=C134816&Units=SI&Type=IR-SPEC&Index=1#IR-SPEC IR], <sup>1</sup>H NMR, [http://www.ebi.ac.uk/nmrshiftdb/portal/js_pane/P-Results/nmrshiftdbaction/showDetailsFromHome/molNumber/10005895 <sup>13</sup>C NMR], MS ([http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP001411 1], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP009582 2], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP010530 3], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP009582 4]).  Also check on [http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng SDBS].
  
 
==From Wikipedia==
 
==From Wikipedia==

Latest revision as of 01:03, 7 September 2010

Structure of benzil Structure of benzil with all atoms shown
  • Main ChemSpider page
  • Molecular formula: C14H10O2
  • Molar mass: 210.228
  • CAS Registry Number: 134-81-6
  • IUPAC name: 1,2-diphenylethane-1,2-dione
  • Appearance: Yellow crystals or powder
  • Melting point: 94-95 °C
  • Solubility properties: Not available
  • Safety sheet: From Oxford University
  • Spectra: IR, 1H NMR, 13C NMR, MS (1, 2, 3, 4). Also check on SDBS.

From Wikipedia

Benzil (systematically known as 1,2-diphenyl-1,2-ethanedione) is the organic compound with the formula (C6H5CO)2, generally abbreviated (PhCO)2. This yellow solid is one of the most common diketones. Its main use is as a photoinitiator in polymer chemistry.[1] Read more... or edit at Wikipedia.

References

  1. Hardo Siegel, Manfred Eggersdorfer "Ketones" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, 2002 by Wiley-VCH, Wienheim. DOI:10.1002/14356007.a15_077