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3-(Trifluoromethyl)phenylacetone

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3-(Trifluoromethyl)phenylacetone Basic information

Product Name:
3-(Trifluoromethyl)phenylacetone
Synonyms:
  • M-(TRIFLUOROMETHYL)PHENYLACETONE
  • 1-(3-Trifluoromethylphenyl)-2-propanone
  • 2-Propanone, 1-(alpha,alpha,alpha-trifluoro-m-tolyl)-
  • m-(Trifluoromethyl)benzyl methyl ketone
  • 3-(TRIFLUORMETHYL)PHENYLACETONE
  • 3-(TRIFLUOROMETHYL)PHENYLACETONE
  • 1-(3-(TRIFLUOROMETHYL)PHENYL)ACETONE
  • 1-(ALPHA,ALPHA,ALPHA-TRIFLUORO-M-TOLYL)-2-PROPANONE
CAS:
21906-39-8
MF:
C10H9F3O
MW:
202.17
EINECS:
244-652-6
Product Categories:
  • Aromatics
  • Building Blocks
  • C10
  • Carbonyl Compounds
  • Chemical Synthesis
  • Ketones
  • Aromatic Ketones (substituted)
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
  • Organic Building Blocks
Mol File:
21906-39-8.mol
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3-(Trifluoromethyl)phenylacetone Chemical Properties

Boiling point:
89-90 °C0.5 mm Hg(lit.)
Density 
1.204 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.457(lit.)
Flash point:
192 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
clear liquid
color 
Light yellow to Amber to Dark green
Specific Gravity
1.204
InChI
InChI=1S/C10H9F3O/c1-7(14)5-8-3-2-4-9(6-8)10(11,12)13/h2-4,6H,5H2,1H3
InChIKey
JPHQCDCEBDRIOL-UHFFFAOYSA-N
SMILES
C(C1=CC=CC(C(F)(F)F)=C1)C(=O)C
CAS DataBase Reference
21906-39-8(CAS DataBase Reference)
NIST Chemistry Reference
2-Propanone, 1-[3-(trifluoromethyl)phenyl]-(21906-39-8)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39
WGK Germany 
3
HS Code 
29147000

MSDS

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3-(Trifluoromethyl)phenylacetone Usage And Synthesis

Chemical Properties

CLEAR YELLOW LIQUID

Uses

3-(Trifluoromethyl)phenylacetone was used in the synthesis of:

  • (±)-[1-(3-trifluoromethyl)phenyl]-2-propylamine via reductive amination reaction
  • N-{2-[1-methyl-2-(3-trifluoromethylphenyl]}-aminoethanol

Synthesis Reference(s)

The Journal of Organic Chemistry, 61, p. 1748, 1996 DOI: 10.1021/jo9518314
Synthesis, p. 474, 1977

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