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Merck

547948

Sigma-Aldrich

α,α,α-Trifluorotoluene

anhydrous, ≥99%

Sinónimos:

Benzotrifluoride

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About This Item

Fórmula lineal:
C6H5CF3
Número de CAS:
Peso molecular:
146.11
Beilstein/REAXYS Number:
1906908
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.21

grade

anhydrous

Quality Level

vapor density

5.04 (vs air)

vapor pressure

38.83 mmHg

assay

≥99%

form

liquid

expl. lim.

0.34-6.3 % (lit.)

technique(s)

NMR: suitable

impurities

≤0.001% water
water

refractive index

n20/D 1.414 (lit.)

bp

102 °C (lit.)

mp

−29 °C (lit.)

density

1.19 g/mL at 20 °C (lit.)

SMILES string

FC(F)(F)c1ccccc1

InChI

1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H

InChI key

GETTZEONDQJALK-UHFFFAOYSA-N

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General description

α,α,α-Trifluorotoluene (TFT) is a potential substitute solvent for reactions carried out in dichloromethane and related solvents. It is also applicable in fluorous synthesis as an organic/fluorous hybrid solvent. TFT undergoes photocycloaddition with cyclopentene to form cyano-substituted tetracyclo[6.3.0.02,11.03,7]undec-9-enes. The nuclear magnetic resonance spectral data of TFT has been reported. The bimolecular rate constants of the aqueous phase reactions between sulfate and phosphate radicals with TFT have been determined by conventional flash-photolysis.

Application

α,α,α-Trifluorotoluene may be used as an internal standard for 19F NMR spectroscopic determination of copper-catalyzed trifluoromethylation of alkenes.

signalword

Danger

Hazard Classifications

Aquatic Chronic 2 - Flam. Liq. 2 - STOT RE 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

46.4 °F - closed cup

flash_point_c

8 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Visite la Librería de documentos

Copper-Catalyzed Trifluoromethylation-Initiated Radical 1,2-Aryl Migration in α,α-Diaryl Allylic Alcohols.
Liu X, et al.
Angewandte Chemie (International Edition in English), 125(27), 7100-7104 (2013)
The meta photocycloaddition of benzonitrile and a,a,a-trifluorotoluene to cyclopentene.
Osselton EM and Cornelisse J.
Tetrahedron Letters, 26(4), 527-530 (1985)
α,α,α-Trifluorotoluene.
Ogawa A and Tsuchii K. <BR/>
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2006)
Reaction of sulfate and phosphate radicals with α,α,α-trifluorotoluene.
Rosso JA, et al.
J. Chem. Soc. Perkin Trans. II, 2, 205-210 (1999)
Nuclear magnetic resonance spectral parameters of α,α,α-trifluorotoluene.
Kostelnik RJ, et al.
Canadian Journal of Chemistry, 47(18), 3313-3318 (1969)

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