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195359

Sigma-Aldrich

4-Fluorobenzotrifluoride

98%

Synonym(s):

α,α,α,4-Tetrafluorotoluene

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5 G
$53.30
25 G
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About This Item

Linear Formula:
FC6H4CF3
CAS Number:
402-44-8
Molecular Weight:
164.10
EC Number:
206-944-1
MDL number:
MFCD00000399
UNSPSC Code:
12352100
PubChem Substance ID:
24851687
NACRES:
NA.22

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Only 5 left in stockDetails
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Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.401 (lit.)

bp

102-105 °C (lit.)

mp

−42-−41.7 °C (lit.)

density

1.293 g/mL at 25 °C (lit.)

functional group

fluoro

SMILES string

Fc1ccc(cc1)C(F)(F)F

InChI

1S/C7H4F4/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H

InChI key

UNNNAIWPDLRVRN-UHFFFAOYSA-N

Related Categories

Application

4-Fluorobenzotrifluoride was used in the synthesis of:
  • 2,2′-bis(trifluoromethylphenoxy)biphenyl via nucleophilic aromatic substitution reaction with 2,2′-biphenol[1]
  • (S)-fluoxetine, potent inhibitor of neuronal serotonin-uptake[2]
  • 1-aryloxy-2-substituted aminomethyltetrahydronaphthalene derivatives[3]

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW9944
MKCV3536
MKCS7617
MKCP7603
MKCN9116

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D W Robertson et al.
Journal of medicinal chemistry, 31(7), 1412-1417 (1988-07-01)
Fluoxetine is a potent and selective inhibitor of the neuronal serotonin-uptake carrier and is a clinically effective antidepressant. Although fluoxetine is used therapeutically as the racemate, there appears to be a small but demonstrable stereospecificity associated with its interactions with
Kalpana Bhandari et al.
Bioorganic & medicinal chemistry, 14(8), 2535-2544 (2005-12-13)
Several 1-aryloxy-2-substituted aminomethyltetrahydronaphthalenes (7-21) as conformationally rigid analogues of fluoxetine were synthesized and evaluated for their anorexigenic and antidepressant activities. For SAR studies the related acyclic analogues (22-27) were also prepared. Out of the 21 synthesized compounds, 10 compounds (9
Akiko Okamoto et al.
Journal of oleo science, 56(9), 479-491 (2007-09-28)
Novel bifunctional acyl-acceptant biphenyls bearing trifluoromethylated aroyloxy groups were successfully synthesized in high yields via TfOH-mediated electrophilic aromatic aroylation of fluorobenzene with CF(3)-bearing aroyl chlorides followed by nucleophilic aromatic substitution with 2,2'-biphenol. Similarly, 2,2'-bis(trifluoromethylphenoxy)biphenyl was synthesized via nucleophilic aromatic substitution

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