ChemicalBook--->CAS DataBase List--->26107-80-2

26107-80-2

26107-80-2 Structure

26107-80-2 Structure
IdentificationMore
[Name]

METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE
[CAS]

26107-80-2
[Synonyms]

3,5-BIS(TRIFLUOROMETHYL)BENZOIC ACID METHYL ESTER
BUTTPARK 89\07-68
METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE
METHYL 3,5-DI(TRIFLUOROMETHYL)BENZOATE
RARECHEM AL BF 0207
Methyl 3,5-bis(trifluoromethyl)benzoate 98%
Methyl3,5-bis(trifluoromethyl)benzoate98%
[EINECS(EC#)]

671-287-3
[Molecular Formula]

C10H6F6O2
[MDL Number]

MFCD00052317
[Molecular Weight]

272.14
[MOL File]

26107-80-2.mol
Chemical PropertiesBack Directory
[Boiling point ]

85 °C
[density ]

1.400±0.06 g/cm3 (20 ºC 760 Torr)
[Fp ]

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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[REACH Registrations]

Inactive
[HS Code ]

2916310090
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Methyl 3,5-bis(trifluoromethyl)benzoate, 98%(26107-80-2)
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

Benzoyl fluoride, 3,5-bis(trifluoromethyl)-

401-96-7

METHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE

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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