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Chemical Structure| 1214-24-0 Chemical Structure| 1214-24-0
Chemical Structure| 1214-24-0

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3,6-Dihydroxyxanthone is a natural compound with antioxidant and anticancer activities. It can scavenge free radicals and show inhibitory effects on various cancer cells.

Synonyms: 3,6-Dihydroxyxanthone

4.5 *For Research Use Only !

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Product Details of 3,6-Dihydroxyxanthone

CAS No. :1214-24-0
Formula : C13H8O4
M.W : 228.20
SMILES Code : O=C1C2=C(OC3=C1C=CC(O)=C3)C=C(O)C=C2
Synonyms :
3,6-Dihydroxyxanthone
MDL No. :MFCD00226967
InChI Key :POARTHFLPKAZBQ-UHFFFAOYSA-N
Pubchem ID :5749322

Safety of 3,6-Dihydroxyxanthone

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of 3,6-Dihydroxyxanthone

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1214-24-0 ]

[ 1214-24-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1214-24-0 ]
  • [ 42019-78-3 ]
  • [ 123853-75-8 ]
 

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Technical Information

• Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Lawesson's Reagent • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Ketenes • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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