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Merck
CN

224936

4-(Trifluoromethyl)aniline

99%

Synonym(s):

α,α,α-Trifluoro-p-toluidine, 4-Aminobenzotrifluoride

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About This Item

Linear Formula:
CF3C6H4NH2
CAS Number:
455-14-1
Molecular Weight:
161.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24853465
EC Number:
207-236-5
Beilstein/REAXYS Number:
1564853
MDL number:
MFCD00064396
Assay:
99%
Form:
liquid

Key Documents

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InChI key

ODGIMMLDVSWADK-UHFFFAOYSA-N

InChI

1S/C7H6F3N/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4H,11H2

SMILES string

Nc1ccc(cc1)C(F)(F)F

assay

99%

form

liquid

Quality Level

200

bp

83 °C/12 mmHg (lit.)

density

1.283 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Related Categories

Application

4-(Trifluoromethyl)aniline was used in the synthesis of 4-(trialkylmethyl)anilines. It was also used as a synthetic building block.

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Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF8284V
WXBF5966V
WXBF3773V
0000226450
0000226498

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Tetrahedron Letters, 48, 4749-4749 (2007)
Meritxell Guinó et al.
The Journal of organic chemistry, 72(16), 6290-6293 (2007-07-13)
Optically active torcetrapib was synthesized in seven steps from achiral precursors without the need for protecting groups, utilizing an enantioselective aza-Michael reaction to achieve asymmetry.
B A Maguire et al.
Biochimica et biophysica acta, 1353(2), 137-147 (1997-08-07)
The rpmB,G operon of Escherichia coli codes for proteins L28 and L33 of the larger (50S) ribosomal subunit. Strains with mutations in this operon can help define the roles of these proteins in ribosome synthesis and function. One such strain
Guiping Ouyang et al.
Molecules (Basel, Switzerland), 10(10), 1351-1357 (2007-11-17)
A facile synthesis of 3-methylthio-3-arylamino-2-cyanoacrylates from 3,3-dimethylthioacrylate and aromatic amines or amino pyridines has been achieved in moderate to high yields (64.0% ~ 93.5%) in 30 minutes at 50 degrees C under microwave irradiation. This method is very simple and
T Kunisawa
Journal of theoretical biology, 213(1), 9-19 (2001-11-16)
A simple method is presented for reconstructing phylogenetic trees on the basis of gene transposition. It is shown that differences in gene arrangements among genomes could allow us to determine whether a gene transposition event has occurred before or after
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