Basic information Safety Supplier Related

4-(TRIFLUOROMETHOXY)BENZYLAMINE

Basic information Safety Supplier Related

4-(TRIFLUOROMETHOXY)BENZYLAMINE Basic information

Product Name:
4-(TRIFLUOROMETHOXY)BENZYLAMINE
Synonyms:
  • 4-(TRIFLUOROMETHOXY)BENZYLAMINE
  • 1-[4-(TRIFLUOROMETHOXY)PHENYL]METHANAMINE
  • P-TRIFLUOROMETHOXYBENZYL AMINE
  • RARECHEM AL BW 0449
  • 4-(Trifluoromethoxy)benzylamine 97%
  • 4-(Trifluoromethoxy)benzylamine97%
  • [4-(Trifluoromethoxy)phenyl]methylamine
  • 4-(Trifluoromethoxy)benzenemethanamine
CAS:
93919-56-3
MF:
C8H8F3NO
MW:
191.15
EINECS:
300-040-1
Product Categories:
  • Fluorine series
  • Amine
  • Amines
  • C8
  • Nitrogen Compounds
Mol File:
93919-56-3.mol
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4-(TRIFLUOROMETHOXY)BENZYLAMINE Chemical Properties

Boiling point:
57-60 °C10 mm Hg(lit.)
Density 
1.252 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.452(lit.)
Flash point:
172 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
8.75±0.10(Predicted)
form 
Liquid
Specific Gravity
1.252
color 
Clear colorless to light yellow
Sensitive 
Air Sensitive
BRN 
8200624
CAS DataBase Reference
93919-56-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,C
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39
RIDADR 
UN2735
WGK Germany 
3
Hazard Note 
Corrosive
HazardClass 
8
PackingGroup 
III
HS Code 
29222990

MSDS

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4-(TRIFLUOROMETHOXY)BENZYLAMINE Usage And Synthesis

Chemical Properties

clear colorless to light yellow liquid

Uses

4-(Trifluoromethoxy)benzylamine may be used in chemical synthesis.

Synthesis

332-25-2

93919-56-3

A tetrahydrofuran (30 mL) solution of 4-(trifluoromethoxy)benzyl cyanide (5.0 g, 26.72 mmol) was slowly added dropwise to a tetrahydrofuran (30 mL) solution of lithium aluminum tetrahydroxide (3.0 g, 88.44 mmol) at 0 °C. After the dropwise addition was completed, the reaction mixture was warmed to room temperature and stirred for 3 hours. Upon completion of the reaction, the mixture was cooled to 4 °C and diluted with tetrahydrofuran (50 mL). Subsequently, the reaction was quenched by sequentially adding water (3 mL), 15% sodium hydroxide solution (3 mL) and water (3 mL). After quenching, the mixture was stirred at room temperature for 15 minutes. The mixture was filtered through diatomaceous earth and the filtrate was dried with anhydrous magnesium sulfate. Finally, the filtrate was concentrated under reduced pressure to give 4-(trifluoromethoxy)benzylamine (3.1 g, 61% yield).

References

[1] Patent: WO2017/139414, 2017, A1. Location in patent: Paragraph 00215-00216

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