Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Hydrocarbons and derivatives >  Aromatic hydrocarbons >  3-(Trifluoromethoxy)iodobenzene

3-(Trifluoromethoxy)iodobenzene

Basic information Safety Supplier Related

3-(Trifluoromethoxy)iodobenzene Basic information

Product Name:
3-(Trifluoromethoxy)iodobenzene
Synonyms:
  • 1-IODO-3-(TRIFLUOROMETHOXY)BENZENE
  • 3-(TRIFLUOROMETHOXY)IODOBENZENE
  • Inter-Iodine Trifluoride Mathoxyphenyl
  • 1-Iodo-3-(trifluoroMethoxy)benzene, 97+%
  • m-iodotrifluoromethoxybenzene
  • 3-Iodo Trifluoromethoxy Benzene
  • 1-Iodo-3-(trifluoromethoxy)benzene 98%
  • 3-Iodophenyl trifluoromethyl ether, 3-Iodo-alpha,alpha,alpha-trifluoroanisole
CAS:
198206-33-6
MF:
C7H4F3IO
MW:
288.01
Product Categories:
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
198206-33-6.mol
More
Less

3-(Trifluoromethoxy)iodobenzene Chemical Properties

Boiling point:
185-186 °C (lit.)
Density 
1.863 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5200(lit.)
Flash point:
135 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light red to Green
Sensitive 
Light Sensitive
CAS DataBase Reference
198206-33-6(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29093090

MSDS

More
Less

3-(Trifluoromethoxy)iodobenzene Usage And Synthesis

Synthesis

1535-73-5

198206-33-6

1. 3-Trifluoromethoxyaniline (17.7 g, 100.00 mmol) was dissolved in H2O (80 ml) at -5 °C and an aqueous solution of NaNO2 (7.4 g, 115.62 mmol) was added. 2. H2SO4 (25 g, 250.00 mmol) was added slowly and dropwise with stirring, keeping the reaction temperature at -5 °C. 3. The reaction mixture was maintained at -5 °C for 15 min. 4. H2O (60 ml) solution of KI (20 g, 120.48 mmol) was added dropwise. 5. The reaction solution was brought to room temperature and stirred overnight. 6. The reaction mixture was extracted with EtOAc (2 x 100 mL). 7. The organic layers were combined, washed with Na2SO3/H2O (2 x 50 mL), dried over Na2SO4 and concentrated in vacuum. 8. The residue was purified by silica gel column chromatography to afford 1-iodo-3-(trifluoromethoxy)benzene (4.0 g, 14% yield).

References

[1] Patent: WO2006/55187, 2006, A1. Location in patent: Page/Page column 99-100

3-(Trifluoromethoxy)iodobenzeneSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.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