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 Chemical Properties
- Melting point:
- 95-98 °C(lit.)
- Boiling point:
- 178 °C / 7mmHg
- Density
- 1.1708 (rough estimate)
- refractive index
- 1.5260 (estimate)
- pka
- 8.03±0.40(Predicted)
- form
- powder to crystal
- color
- Light yellow to Yellow to Orange
- BRN
- 1238635
- InChIKey
- LLBBBYLDTDJMNU-UHFFFAOYSA-N
- CAS DataBase Reference
- 5792-36-9(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
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2',4'-Dihydroxypropiophenone Usage And Synthesis
Chemical Properties
light yellow crystals or crystalline powder
Preparation
Preparation 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%).
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