4-(Trifluoromethoxy)benzonitrile
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
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)
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
- Language:English Provider:4-(Trifluoromethoxy)benzonitrile
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
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4-(Trifluoromethoxy)benzonitrile(332-25-2)Related Product Information
- Anisole
- p-Anisaldehyde
- 4-Methoxybenzoic acid
- 2-(Trifluoromethoxy)aniline
- m-Anisyl alcohol
- 4-(Trifluoromethoxy)chlorobenzene
- 4'-(Trifluoromethoxy)acetophenone
- (Trifluoromethoxy)benzene
- 4-(Trifluoromethoxy)benzaldehyde
- 4-Methoxybenzyl cyanide
- 3-(METHOXYMETHOXY)BENZALDEHYDE
- 3-(Trifluoromethoxy)aniline
- o-Anisaldehyde
- p-Trifluoromethoxy phenol
- 4-(Trifluoromethoxy)aniline
- 4-Methoxyphenylacetic acid
- Benzonitrile
- Trifluoro-p-tolunitrile