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- Q415920 subject Q7137781.
- Q415920 subject Q7308299.
- Q415920 subject Q7321877.
- Q415920 abstract "Pyridinium chlorochromate (PCC) is a red–orange salt with the formula C5H5NH[CrO3Cl]. It is a reagent in organic synthesis used primarily for the oxidation of alcohols to form carbonyls. A variety of related compounds are known with similar reactivity. Although no longer widely used, PCC offered the advantage of the selective oxidation of alcohols to aldehydes, whereas many other reagents were less selective. Disadvantages to using PCC are the tedious reaction workup and its toxicity. The chemical was first synthesized and used by E.J. Corey and J. William Suggs.".
- Q415920 iupacName "Pyridinium chlorochromate".
- Q415920 thumbnail Pyridinium_chlorochromate.PNG?width=300.
- Q415920 wikiPageExternalLink chromium.html.
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- Q415920 wikiPageExternalLink PCCDevelopment.html.
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- Q415920 wikiPageWikiLink Q7137781.
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- Q415920 wikiPageWikiLink Q7308299.
- Q415920 wikiPageWikiLink Q7321877.
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- Q415920 iupacname "Pyridinium chlorochromate".
- Q415920 name "Pyridinium chlorochromate".
- Q415920 type ChemicalCompound.
- Q415920 type ChemicalSubstance.
- Q415920 type ChemicalObject.
- Q415920 type Thing.
- Q415920 type Q11173.
- Q415920 comment "Pyridinium chlorochromate (PCC) is a red–orange salt with the formula C5H5NH[CrO3Cl]. It is a reagent in organic synthesis used primarily for the oxidation of alcohols to form carbonyls. A variety of related compounds are known with similar reactivity. Although no longer widely used, PCC offered the advantage of the selective oxidation of alcohols to aldehydes, whereas many other reagents were less selective. Disadvantages to using PCC are the tedious reaction workup and its toxicity.".
- Q415920 label "Pyridinium chlorochromate".
- Q415920 depiction Pyridinium_chlorochromate.PNG.
- Q415920 name "Pyridinium chlorochromate".