4-(TRIFLUOROACETYL)TOLUENE
4-(TRIFLUOROACETYL)TOLUENE Basic information
- Product Name:
- 4-(TRIFLUOROACETYL)TOLUENE
- Synonyms:
-
- (Trifluoromethyl)-p-tolylketone
- Ethanone,2,2,2-trifluoro-1-(4-methylphenyl)-
- 4-(TRIFLUOROACETYL)TOLUENE
- 2,2,2-TRIFLUORO-1-(P-TOLYL)ETHANONE
- 4-(Trifluoroacetyl)toluene97.
- 4'-Methyl-2,2,2-trifluoroacetophenone 97%
- 4'-Methyl-2,2,2-trifluoroacetophenone 4-(Trifluoroacetyl)toluene
- 4-(Trifluoroacetyl)toluene, 1-(4-Methylphenyl)-2,2,2-trifluoroethan-1-one
- CAS:
- 394-59-2
- MF:
- C9H7F3O
- MW:
- 188.15
- Mol File:
- 394-59-2.mol
4-(TRIFLUOROACETYL)TOLUENE Chemical Properties
- Melting point:
- 5°C
- Boiling point:
- 70 °C
- Density
- 1.2304 g/cm3(Temp: 25 °C)
- refractive index
- 1.47
- Flash point:
- 70-72°C/15mm
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
- form
- clear liquid
- color
- Colorless to Light yellow to Light orange
- BRN
- 1870406
- CAS DataBase Reference
- 394-59-2(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39-37
- HazardClass
- IRRITANT
- HS Code
- 29039990
MSDS
- Language:English Provider:ALFA
4-(TRIFLUOROACETYL)TOLUENE Usage And Synthesis
Chemical Properties
Clear colorless to light yellow liquid
Uses
p-Trifluoroacetyltoluene is used as a reagent in the synthesis of 5-methylene-2-(trifluoromethyl)morpholin-3-one derivatives which have fungicidal activity.
Synthesis
In a nitrogen atmosphere, one PTFE magnet was placed in a reactor, and 0.4 mmol p-methylbenzene diazonium tetrafluoroborate, 0.1 mmol cuprous oxide, 1 , 0.8 mmol dimethyl sulfoxide, and finally 1.2 mmol ethyl trifluoropyruvate were added. mL of dichloromethane, 0.8 mmol of dimethyl sulfoxide, and finally 1.2 mmol of ethyl trifluoropyruvate were added, and the reaction was stirred at 25 ??C for 16 in a closed system. After h, the reaction was extracted with ether 3 times, 10 mL each time, the organic phases were combined and washed with distilled water 3 times, the organic phase was dried with anhydrous magnesium sulfate, filtered, and then rotary evaporated to remove the organic solvent . The obtained crude product was eluted by silica gel column chromatography with n-pentane as eluent to obtain 4-(trifluoroacetyl)toluene (86% isolated yield).
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4-(TRIFLUOROACETYL)TOLUENE(394-59-2)Related Product Information
- 4-(TRIFLUOROACETYL)TOLUENE
- 4-(TRIFLUOROACETYL)BENZOIC ACID
- 4'-Methylacetophenone
- Trifluoroacetophenone
- 4'-TERT-BUTYL-2,2,2-TRIFLUOROACETOPHENONE
- 1-(3-CHLORO-4-METHYL-PHENYL)-2,2,2-TRIFLUORO-ETHANONE
- 3'-FLUORO-4'-METHYL-2,2,2-TRIFLUOROACETOPHENONE
- Ethanone, 1-(3,4-dimethylphenyl)-2,2,2-trifluoro- (9CI)
- Ethanone, 2,2,2-trifluoro-1-(4-propylphenyl)- (9CI)
- 4'-N-BUTYL-2,2,2-TRIFLUOROACETOPHENONE
- Ethanone, 1-(2,4-dimethylphenyl)-2,2,2-trifluoro- (9CI)
- Ethanone, 2,2,2-trifluoro-1-[4-(1-methylethyl)phenyl]- (9CI)
- Ethanone, 1-(4-ethylphenyl)-2,2,2-trifluoro- (9CI)
- 4'-CYANO-2,2,2-TRIFLUOROACETOPHENONE
- 4-(TRIFLUOROMETHYL)-ALPHA,ALPHA,ALPHA-TRIFLUOROACETOPHENONE
- 1-(4-METHYLNAPHTHYL) TRIFLUOROMETHYL KETONE
- 2,2,2-TRIFLUORO-1-(4-PENTYL-PHENYL)-ETHANONE
- P-DECYL-A,A,A-TRIFLUOROACETOPHENONE