2',4'-Dihydroxypropiophenone

2',4'-Dihydroxypropiophenone Basic information
Product Name:2',4'-Dihydroxypropiophenone
Synonyms:2,4-DIHYDROXYPHENYL ETHYL KETONE;2',4'-DIHYDROXYPROPIOPHENONE;2,4-DIHYDROXYPROPIOPHENONE;1-(2,4-DIHYDROXYPHENYL)PROPAN-1-ONE;2',4'-Dihydroxypropiophenone,99%;ETHYL 2,4-DIHYDROXYPHENYL KETONE;4-PROPIONYLRESORCINOL;LABOTEST-BB LT00261298
CAS:5792-36-9
MF:C9H10O3
MW:166.17
EINECS:227-329-4
Product Categories:Aromatic Propiophenones (substituted);C9;Carbonyl Compounds;Ketones
Mol File:5792-36-9.mol
2',4'-Dihydroxypropiophenone Structure
2',4'-Dihydroxypropiophenone Chemical Properties
Melting point 95-98 °C(lit.)
Boiling point 178 °C / 7mmHg
density 1.1708 (rough estimate)
refractive index 1.5260 (estimate)
pka8.03±0.40(Predicted)
form powder to crystal
color Light yellow to Yellow to Orange
BRN 1238635
InChIKeyLLBBBYLDTDJMNU-UHFFFAOYSA-N
CAS DataBase Reference5792-36-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-24/25
WGK Germany 3
HS Code 29145090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2',4'-Dihydroxypropiophenone Usage And Synthesis
Chemical Propertieslight yellow crystals or crystalline powder
PreparationPreparation by reaction of propionic acid with resorcinol,
in the presence of zinc chloride (Nencki reaction), at reflux (160–165°) ? for 15 min, at 150° for 20 min
in the presence of boron trifluoride for 2 h at 70° (79%), at 80° (67%) ? or at 105–108° for 15 min (71%)
in the presence of polyphosphoric acid for 10–20 min in a boiling water bath ? (65%)
in the presence of 70% perchloric acid at reflux for 30 min (70%)
in the presence of Amberlite IR-120 (cation exchange resin sulfonic acid type) ? at 160° for 2–3 h (76%)
Preparation by reaction of propionitrile with resorcinol (Hoesch reaction) (75%) (65%) (46%)(35%)
Preparation by reaction of propionic anhydride with resorcinol
in the presence of Amberlite IR-120 (cation exchange resin sulfonic acid ? type) at 160° for 2–3 h (82%)
in the presence of concentrated sulfuric acid (small drops) at 130° for some ? min (60%)
Also obtained by Fries rearrangement of resorcinol dipropionate
with aluminium chloride at 180–185° for 90 min (25%)
with boron trifluoride, in the presence of resorcinol, at 75° for 1 h (83%)
Also obtained by reaction of ethylmagnesium bromide with 2,4-dihydroxy-N, N-diethylbenzamide in refluxing benzene (12%).









2',4'-Dihydroxypropiophenone Preparation Products And Raw materials
Raw materialsResorcinol
Prunetin 2-CARBETHOXY-5,7-DIHYDROXY-4'-METHOXYISOFLAVONE Phlorizin 4-Hexanoylresorcinol 2',4'-Dihydroxypropiophenone Phloretin Naringenin Genistein Rotenone Triclosan 2',4'-DIHYDROXY-3'-METHYLPROPIOPHENONE Daidzein 3'-Hydroxypropiophenone (+)-TAXIFOLIN 4'-Methylpropiophenone 5,7-Dihydrox -4'-methoxyisoflavone Propiophenone Genistin

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