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3,5-Bis(trifluoromethyl)aniline

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3,5-Bis(trifluoromethyl)aniline Basic information

Product Name:
3,5-Bis(trifluoromethyl)aniline
Synonyms:
  • ,,,’,’,’-Hexafluoro-3,5-xylidine
  • ,5-Bis-trifluoromethyl-phenylamine
  • ,5-Xylidine, a,a,a,a',a',a'-hexafluoro-
  • ,a,a,a',a',a'-Hexafluoro-3,5-xylidine
  • 3,5-bis(trifluoromethyl)-anilin
  • 3,5-bis(trifluoromethyl)-benzenamin
  • 3,5-Bis(trifluoromethyl)benzenamine
  • 3,5-Di(trifluorometh
CAS:
328-74-5
MF:
C8H5F6N
MW:
229.12
EINECS:
206-335-0
Product Categories:
  • Aniline series
  • Fluorobenzene
  • Trifluoromethylbenzene serise
  • Anilines, Aromatic Amines and Nitro Compounds
  • Miscellaneous
Mol File:
328-74-5.mol
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3,5-Bis(trifluoromethyl)aniline Chemical Properties

Melting point:
168.2-169.2 °C
Boiling point:
85 °C15 mm Hg(lit.)
Density 
1.467 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.434(lit.)
Flash point:
182 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Liquid
pka
2.15±0.10(Predicted)
Specific Gravity
1.473
color 
Clear light yellow to yellow-brown
Water Solubility 
Not miscible in water.
BRN 
654318
InChIKey
CDIDGWDGQGVCIB-UHFFFAOYSA-N
CAS DataBase Reference
328-74-5(CAS DataBase Reference)
NIST Chemistry Reference
Benzenamine, 3,5-bis(trifluoromethyl)-(328-74-5)
EPA Substance Registry System
Benzenamine, 3,5-bis(trifluoromethyl)- (328-74-5)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
33-36/37/38-20/21/22
Safety Statements 
26-36/37/39-36
RIDADR 
2810
WGK Germany 
3
RTECS 
ZE9800000
Hazard Note 
Irritant
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29214910

MSDS

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3,5-Bis(trifluoromethyl)aniline Usage And Synthesis

Chemical Properties

clear light yellow to yellow-brown liquid

Uses

3,5-Bis(trifluoromethyl)aniline was found to be a highly efficient monodentate transient directing group (MonoTDG) for the palladium-catalyzed direct dehydrogenative cross-coupling of benzaldehydes with arenes.

Synthesis

The synthesis of 3,5-Bis(trifluoromethyl)aniline is as follows is as follows:Put 259g (1mol) 3,5-Bis(trifluoromethyl)nitrobenzeneand 500g ethyl acetate into a 1L autoclave, add 5g palladium-carbon as a catalyst, raise the temperature to 60℃, then pass the hydrogen pressure to 2MPa, keep the temperature and react for 20 hours, then cooling, filtration, concentration, and distillation to obtain 3,5-Bis(trifluoromethyl)aniline with a purity of 98.5% and a yield of 87%.

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