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Open Access Articles- Top Results for Tropolone

Tropolone

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Tropolone[1]

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This page is a soft redirect. Names

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IUPAC name
2-Hydroxy-2,4,6-cycloheptatrien-1-one
Other names
2-Hydroxytropone; Purpurocatechol
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533-75-5 7pxY ChEMBL ChEMBL121188 7pxN ChemSpider 10333 7pxN EC number 208-577-2 Jmol-3D images Image KEGG C15474 7pxN MeSH D014334 PubChem Template:Chembox PubChem/format Template:Chembox UNII colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Properties

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C7H6O2 Molar mass 122.12 g/mol Melting point Script error: No such module "convert". Boiling point Script error: No such module "convert". (0.1 mmHg) Acidity (pKa) 6.89 (and -0.5 for conjugate acid) colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Hazards

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S-phrases S22 S24/25 Flash point Script error: No such module "convert". colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Related compounds

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Related compounds
Hinokitiol (4-isopropyl-tropolone)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tropolone is a derivative of tropone with a hydroxyl group in the 2-position.

Two methods for the synthesis of tropolone are by bromination of 1,2-cycloheptanedione with N-bromosuccinimide followed by dehydrohalogenation at elevated temperatures and by acyloin condensation of the ethyl ester of pimelic acid the acyloin again followed by oxidation by bromine.

It is a grape polyphenol oxidase inhibitor.[2]

[3]

References

  1. ^ Tropolone at Sigma-Aldrich
  2. ^ Time-dependent inhibition of grape polyphenol oxidase by tropolone. Edelmira Valero, Manuela Garcia-Moreno, Ramon Varon and Francisco Garcia-Carmona, J. Agric. Food Chem., 1991, 39 (6), pp 1043–1046, doi:10.1021/jf00006a007
  3. ^ Chedgy, Russell. Secondary metabolites of Western red cedar (Thuja plicata): their biotechnological applications and role in conferring natural durability. LAP Lambert Academic Publishing, 2010, ISBN 3-8383-4661-0, ISBN 978-3-8383-4661-8