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3-(3-(Trifluoromethyl)phenyl)propanal

Basic information Uses Safety Supplier Related

3-(3-(Trifluoromethyl)phenyl)propanal Basic information

Product Name:
3-(3-(Trifluoromethyl)phenyl)propanal
Synonyms:
  • 3-(3-TRIFLUOROMETHYL-PHENYL)-PROPIONALDEHYDE
  • 3-(Trifluoromethyl)benzenepropanal
  • m-(Trifluoromethyl)hydrocinnamaldehyde
  • 4-[3-(trifluoroMethyl)phenyl]butanal
  • Benzenepropanal, 3-(trifluoroMethyl)-
  • 3-(trifluoroMethylphenyl)propionaldehyde
  • 3-(3-(trifluoroMethyl)phenyl)propanal
  • 3-(3-TRIFLUOROMETHYL-PHENYL)-PROPIOLDEHYDE
CAS:
21172-41-8
MF:
C10H9F3O
MW:
202.17
EINECS:
606-717-0
Product Categories:
  • Cinacalcet Intermediate
  • Aromatics Compounds
  • Aromatics
Mol File:
21172-41-8.mol
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3-(3-(Trifluoromethyl)phenyl)propanal Chemical Properties

Boiling point:
207.4±35.0 °C(Predicted)
Density 
1.192±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Soluble in Chloroform, Dichloromethane, Ethyl acetate
form 
Oil
color 
Clear colorless to pale yellow oily liquid
Stability:
Not very stable, new spot on TLC if kept at r.t. o/n.
InChI
InChI=1S/C10H9F3O/c11-10(12,13)9-5-1-3-8(7-9)4-2-6-14/h1,3,5-7H,2,4H2
InChIKey
APCCHYPQHODSBD-UHFFFAOYSA-N
SMILES
C1(CCC=O)=CC=CC(C(F)(F)F)=C1
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Safety Information

HS Code 
2912490090
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3-(3-(Trifluoromethyl)phenyl)propanal Usage And Synthesis

Uses

3-(Trifluoromethyl)benzenepropanal is a compound useful in organic synthesis.

Chemical Properties

Colourless Oil

Uses

3-(Trifluoromethyl)benzenepropanal (cas# 21172-41-8) is a compound useful in organic synthesis.

Synthesis

A solution of 3-(Trifluoromethyl) benzene propanol (1.0 g, 4.90 mmol) in dichloromethane (20 ml) is cooled in a water/ice bath, treated in succession with DMSO (770 mg, 9.80 mmol) and P2O5 (1.39 g, 9.80 mmol) and left under stirring for 30 minutes, while temperature raises to 20°C. The reaction mixture is then cooled in water/ice bath and triethylamine (2.4 ml, 17.15 mmol). The resulting solution is kept under stirring while the temperature raises to 20°C. After one hour, the mixture is treated with 5 per cent HCl, the phases are separated, and the organic one is further washed with 5 per cent HCl. The organic phase is then washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to afford 0.99 g of the aldehyde of 3-(3-(Trifluoromethyl)phenyl)propanal in quantitative yield.

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