Basic information Safety Supplier Related

METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE

Basic information Safety Supplier Related

METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE Basic information

Product Name:
METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE
Synonyms:
  • RARECHEM AL BF 0207
  • BUTTPARK 89\07-68
  • METHYL 3,5-DI(TRIFLUOROMETHYL)BENZOATE
  • METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE
  • 3,5-BIS(TRIFLUOROMETHYL)BENZOIC ACID METHYL ESTER
  • Methyl 3,5-bis(trifluoromethyl)benzoate 98%
  • Methyl3,5-bis(trifluoromethyl)benzoate98%
  • Methyl 3,5-bis(trifluoromethyl)
CAS:
26107-80-2
MF:
C10H6F6O2
MW:
272.14
EINECS:
671-287-3
Product Categories:
  • Benzoic acid
Mol File:
26107-80-2.mol
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METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE Chemical Properties

Boiling point:
85 °C
Density 
1.400±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
85-87°C/15mm
storage temp. 
Sealed in dry,Room Temperature
Appearance
Colorless to light yellow Liquid
CAS DataBase Reference
26107-80-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
Hazard Note 
Irritant
HS Code 
2916310090

MSDS

  • Language:English Provider:ALFA
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METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE Usage And Synthesis

Synthesis

67-56-1

401-96-7

26107-80-2

To the reaction system was added 25.9 g (0.8 mol) of methanol, and after chlorine-fluorine exchange using HF according to the method of Example 2, 13.8 g (0.053 mol) of 3,5-bis(trifluoromethyl)benzoyl fluoride fraction was obtained, which was added slowly and dropwise to the reaction system over 60 minutes. Subsequently, the reaction mixture was stirred at 40°C for 4 hours. The generation of 14.2 g (0.052 mol) of methyl 3,5-bis(trifluoromethyl)benzoate was confirmed by gas chromatographic analysis (yield: 98%, selectivity: 100%). By vacuum distillation, 13.9 g (0.05 mol) of methyl 3,5-bis(trifluoromethyl)benzoate was isolated (yield: 96%). Examples 17-31 Various (fluoroalkyl)benzene derivatives were prepared with reference to the methods of Examples 2-16. To improve the purity of the product, Example 17 was purified by crystallization twice, and the final distillation step was repeated in the remaining Examples. The purity, residual halogen content and residual metal content of all (fluoroalkyl)benzene derivatives are summarized in Table 2.

References

[1] Patent: EP1500641, 2005, A1. Location in patent: Page 10; 15

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