3',4'-Difluoroacetophenone
3',4'-Difluoroacetophenone Basic information
- Product Name:
- 3',4'-Difluoroacetophenone
- Synonyms:
-
- 1-(3,4-Difluorophenyl)ethan-1-one
- 1-(3,4-DIFLUORO-PHENYL)-ETHANONE
- 3,4-DIFLUOROACETOPHENONE
- OTAVA-BB BB7020410077
- Ethanone, 1-(3,4-difluorophenyl)-
- 3,4-Difluoroacetophenone,98%
- 3',4'-Difluoro
- 3',4'-Difluoroacetophenone 99%
- CAS:
- 369-33-5
- MF:
- C8H6F2O
- MW:
- 156.13
- EINECS:
- 206-717-7
- Product Categories:
-
- Acetophenone Series
- Aromatic Acetophenones & Derivatives (substituted)
- ketone
- Miscellaneous
- Adehydes, Acetals & Ketones
- Fluorine Compounds
- C7 to C8
- Carbonyl Compounds
- Ketones
- bc0001
- Mol File:
- 369-33-5.mol
3',4'-Difluoroacetophenone Chemical Properties
- Melting point:
- 19-20 °C(lit.)
- Boiling point:
- 94-95 °C13 mm Hg(lit.)
- Density
- 1.246 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.4916(lit.)
- Flash point:
- 167 °F
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to lump to clear liquid
- color
- White or Colorless to Light yellow
- Specific Gravity
- 1.246
- Water Solubility
- INSOLUBLE
- BRN
- 2206856
- InChIKey
- VWJSSJFLXRMYNV-UHFFFAOYSA-N
- CAS DataBase Reference
- 369-33-5(CAS DataBase Reference)
- NIST Chemistry Reference
- 3',4'-Difluoroacetophenone(369-33-5)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29147000
MSDS
- Language:English Provider:1-(3,4-Difluorophenyl)ethan-1-one
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
3',4'-Difluoroacetophenone Usage And Synthesis
Chemical Properties
clear yellowish liquid after melting
Uses
3′,4′-Difluoroacetophenone may be used in chemical synthesis.
Definition
ChEBI: 1-(3,4-Difluorophenyl)ethan-1-one is an aromatic ketone.
Synthesis
367-11-3
75-36-5
369-33-5
Anhydrous aluminum trichloride (117 g) was slowly added to a mixed solution of 1,2-difluorobenzene (50 g) with acetyl chloride (86 g) at room temperature. The formed slurry was heated to 30°C with continuous stirring. Upon completion of the reaction, the red reaction mixture was cooled to 20 °C and subsequently slowly poured into 800 g of ice-water mixture with continued stirring for 30 min. The organic phase was separated and the aqueous phase was extracted with dichloromethane (3 x 500 ml). All organic phases were combined and washed sequentially with water (2 x 500 ml), saturated sodium bicarbonate solution (2 x 500 ml) and 15% brine (2 x 500 ml), followed by drying with anhydrous sodium sulfate. The organic phases were concentrated to remove the solvent and finally distilled under reduced pressure to collect the fractions at 95 °C/13 mmHg to give 3',4'-difluoroacetophenone (51 g).
References
[1] Journal of Fluorine Chemistry, 1980, vol. 15, p. 245 - 252
[2] Journal of the Indian Chemical Society, 1982, vol. 59, # 2, p. 293 - 294
[3] Heterocycles, 1981, vol. 16, # 9, p. 1545 - 1553
[4] Journal of Medicinal Chemistry, 1979, vol. 22, # 11, p. 1385 - 1389
[5] Heterocycles, 1981, vol. 16, # 1, p. 71 - 76
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3',4'-Difluoroacetophenone (369-33-5)Related Product Information
- 4'-Methylacetophenone
- Trifluoroacetophenone
- 4'-(Trifluoromethyl)acetophenone
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- 4'-Hydroxyacetophenone
- 4-Nitroacetophenone
- 3'-Fluoroacetophenone
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- PIPERACETAZINE (250 MG)
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