Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Organic fluorine compound >  Fluorobenzonitrile series >  4-(Trifluoromethoxy)benzonitrile

4-(Trifluoromethoxy)benzonitrile

Basic information Safety Supplier Related

4-(Trifluoromethoxy)benzonitrile Basic information

Product Name:
4-(Trifluoromethoxy)benzonitrile
Synonyms:
  • 4-(trifluoromethoxy)benzonitrile(SALTDATA: FREE)
  • For trifluoromethoxy benzene nitrile
  • 4-(TRIFLUOROMETHOXY)BENZONITRILE 98
  • 4-(Trifluoromethoxy)benzonitrile 98%
  • p-trifluoromethoxybenonitrile
  • 4-(Trifluoromethoxy)benzonitrile
  • p-Cyanotrifluoromethoxybenzene
  • Benzonitrile, 4-(trifluoromethoxy)-
CAS:
332-25-2
MF:
C8H4F3NO
MW:
187.12
EINECS:
206-363-3
Product Categories:
  • Trifluoroanisole series
  • Aromatic Nitriles
  • Building Blocks
  • C8 to C9
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Nitrile
  • C8 to C9
  • Cyanides/Nitriles
  • Nitrogen Compounds
Mol File:
332-25-2.mol
More
Less

4-(Trifluoromethoxy)benzonitrile Chemical Properties

Boiling point:
192-193 °C(lit.)
Density 
1.285 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.452(lit.)
Flash point:
181 °F
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
color 
Colorless to Almost colorless
BRN 
2832939
InChI
InChI=1S/C8H4F3NO/c9-8(10,11)13-7-3-1-6(5-12)2-4-7/h1-4H
InChIKey
XWHIXOMWXCHJPP-UHFFFAOYSA-N
SMILES
C(#N)C1=CC=C(OC(F)(F)F)C=C1
CAS DataBase Reference
332-25-2(CAS DataBase Reference)
EPA Substance Registry System
Benzonitrile, 4-(trifluoromethoxy)- (332-25-2)
More
Less

Safety Information

Hazard Codes 
Xn,T,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37/39-45
RIDADR 
3276
WGK Germany 
3
Hazard Note 
Toxic
HazardClass 
6.1
PackingGroup 
III
HS Code 
29269090

MSDS

More
Less

4-(Trifluoromethoxy)benzonitrile Usage And Synthesis

Chemical Properties

clear light yellow liquid

General Description

4-(Trifluoromethoxy)benzonitrile serves as an intermediate in the synthesis of fluvoxamine.

Synthesis

1736-74-9

332-25-2

To a 25 mL Schlenk tube equipped with a magnetic stirrer were sequentially added CuCl (0.05 mmol, 5 mol%), DABCO (0.10 mmol, 10 mol%) and 4-HO-TEMPO (0.05 mmol, 5 mol%). Subsequently, a solution of acetonitrile (2 mL) with 4-trifluoromethoxybenzyl alcohol (1 mmol) and ammonia (25-28%, 3 mmol, 3.0 equiv) was added. The reaction mixture was stirred at room temperature for 24 h under balloon protection. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was diluted with water and extracted with ethyl acetate. The organic layers were combined and dried with anhydrous magnesium sulfate. After concentration under reduced pressure, the crude product was purified by column chromatography to give p-trifluoromethoxybenzonitrile.

References

[1] Advanced Synthesis and Catalysis, 2014, vol. 356, # 18, p. 3892 - 3896
[2] Chinese Chemical Letters, 2018, vol. 29, # 3, p. 464 - 466

4-(Trifluoromethoxy)benzonitrileSupplier

Shanghai Harvest Chemical Industrial Co., Ltd. Gold
Tel
021-31038972,31038973 17321035817
Email
sales@harvest-chem.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Email
sales@demochem.com