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Chemical Structure| 89-84-9 Chemical Structure| 89-84-9
Chemical Structure| 89-84-9

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2,4-Dihydroxyacetophenone is a natural product isolated and purified from the root of Paeonia moutan Sim..

Synonyms: Resacetophenone; 1-(2,4-Dihydroxyphenyl)ethanone; 4-Acetylresorcinol

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Product Details of 2',4'-Dihydroxyacetophenone

CAS No. :89-84-9
Formula : C8H8O3
M.W : 152.15
SMILES Code : CC(C1=CC=C(O)C=C1O)=O
Synonyms :
Resacetophenone; 1-(2,4-Dihydroxyphenyl)ethanone; 4-Acetylresorcinol
MDL No. :MFCD00002279
InChI Key :SULYEHHGGXARJS-UHFFFAOYSA-N
Pubchem ID :6990

Safety of 2',4'-Dihydroxyacetophenone

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2',4'-Dihydroxyacetophenone

* 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 [ 89-84-9 ]

[ 89-84-9 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 89-84-9 ]
  • [ 3847-57-2 ]
  • 7-acetoxy-4-methyl-3-(4-nitro-phenyl)-coumarin [ No CAS ]
  • 2
  • [ 89-84-9 ]
  • [ 1818-27-5 ]
  • 3
  • [ 89-84-9 ]
  • [ 3381-87-1 ]
  • [ 103633-37-0 ]
  • [ 103633-36-9 ]
  • 4
  • [ 89-84-9 ]
  • [ 1202-25-1 ]
  • 1-(2,4-Dihydroxy-phenyl)-3-(4-dimethylamino-phenyl)-propane-1,3-dione [ No CAS ]
  • 7
  • [ 123-75-1 ]
  • [ 7731-02-4 ]
  • [ 89-84-9 ]
  • [ 62756-43-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In toluene; EXAMPLE 31 304 g of 2,4-dihydroxy-acetophenone and 142 g of pyrrolidine are stirred in 1 l of toluene. 320 g of 1-N-pyrrolidinyl-cyclohexane are then added and the mixture is stirred for 3 hours at 25 and then for a further 3 hours at the reflux temperature. After cooling, 1 kg of ice and 1 l 4 N HCl are stirred into the dark solution. After a short time 2,2-pentamethylene-7-hydroxychroman-4-one precipitates out from the organic phase and is filtered off and rinsed with water. The toluene is separated off from the filtrate and concentrated to about 400 ml, whereupon a further fraction precipitates. Total yield 339 g (73% of the theoretical yield): melting point: 170-171.
  • 8
  • [ 89-84-9 ]
  • [ 4876-10-2 ]
  • [ 1299366-58-7 ]
  • 9
  • [ 89-84-9 ]
  • [ 1668-54-8 ]
  • [ 1465740-19-5 ]
  • 10
  • [ 40915-37-5 ]
  • [ 89-84-9 ]
  • C20H24O5 [ No CAS ]
  • 11
  • [ 89-84-9 ]
  • [ 34800-90-3 ]
  • C20H18N2O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
73.0% In ethanol;Reflux; General procedure: solutionof acid hydrazide (0.01 mol) and appropriate benzaldehyde/acetophenone (0.01 mol) in ethanol was refluxed for 5-6 h. The precipitated title compounds were then filtered off, washed with water and recrystallized from ethanol.
  • 12
  • [ 41014-43-1 ]
  • [ 89-84-9 ]
  • 1-(4-(benzo[d]oxazol-2-ylmethoxy)-2-hydroxyphenyl)ethanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
31.8% With potassium carbonate; In acetone; for 4h;Reflux; General procedure: To a solution of various substituted phenols (1 mmol) in dry acetone (30 mL) K2CO3 (1 mmol)and compound 3 or 4 (1 mmol) were added. After being stirred for 4 h at reflux temperature, thereaction mixture was cooled, filtered, and concentrated under vacuum. Then the residue was dilutedwith 30 mL ethyl acetate and sequentially washed with 30 mL 1 M HCl, aq. NaHCO3 solution andbrine in order. The organic layer was dried over MgSO4 and concentrated in vacuo. Purification of theresidue by chromatography on silica gel furnished target compounds. 1H-NMR, 13C-NMR and massspectroscopy (MS) of compounds 5a-m and 6a-m are shown in Supplementary Materials.
  • 13
  • [ 89-84-9 ]
  • [ 1671-88-1 ]
  • 6-(2,4-dihydroxyphenyl)-3-(pyridin-2-yl)-7H-pyrido[2,1-d][1,2,4]triazolo[4,3-b][1,2,5]triazepin-8-ium iodide [ No CAS ]
 

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