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2-(Trifluoromethyl)aniline

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Identification
Molecular formula
C7H6F3N
CAS number
88-17-5
IUPAC name
2-(trifluoromethyl)aniline
State
State
At room temperature, 2-(trifluoromethyl)aniline is a liquid. It has a distinct aromatic odor typical of anilines.
Melting point (Celsius)
5.50
Melting point (Kelvin)
278.65
Boiling point (Celsius)
159.00
Boiling point (Kelvin)
432.15
General information
Molecular weight
161.14g/mol
Molar mass
161.1410g/mol
Density
1.3520g/cm3
Appearence

2-(Trifluoromethyl)aniline typically appears as a colorless to pale yellow liquid. In its pure form, it can be clear and transparent but can acquire a slight yellow tint upon exposure to air due to oxidation.

Comment on solubility

Solubility of 2-(trifluoromethyl)aniline

2-(Trifluoromethyl)aniline is a fascinating compound when it comes to solubility due to its unique structural features. Understanding its solubility characteristics can be examined through the following points:

  • Organic Solvents: This compound typically exhibits good solubility in organic solvents such as ethanol, methanol, and various aromatic hydrocarbons.
  • Water Solubility: Its water solubility is quite limited. This can be attributed to the presence of the bulky trifluoromethyl group, which hinders strong interactions with water molecules.
  • pH Sensitivity: The solubility may also vary with pH, as it can form ionic species under certain conditions, affecting its overall solubility profile.

In summary, while C7H6F3N is soluble in many organic mediums, its performance in aqueous environments is significantly reduced, making it crucial to consider the solvent when working with this particular aniline derivative.

Interesting facts

Interesting Facts About 2-(Trifluoromethyl)aniline

2-(Trifluoromethyl)aniline, often abbreviated as TFM-aniline, is a fascinating compound in the realm of organic chemistry. This aromatic amine exhibits unique properties and applications, making it of interest to both researchers and industry professionals. Here are some noteworthy points to consider:

  • Fluorine's Influence: The presence of the trifluoromethyl group enhances the compound's electrical properties, leading to increased lipophilicity and improved interaction with biological targets.
  • Applications: This compound is primarily utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its chemical versatility enables it to serve as an essential building block in complex molecular architectures.
  • Reactivity: The electron-withdrawing nature of the trifluoromethyl group can affect reactivity, often making TFM-aniline behave differently than its less-substituted counterparts. This characteristic is crucial for predicting reaction outcomes in synthetic pathways.
  • Toxicity Considerations: Like many fluorinated compounds, care must be taken when handling TFM-aniline due to potential toxicity. It’s important for scientists to follow proper safety protocols when working with such materials.
  • Research Interest: Ongoing studies investigate the compound's behaviour in various biochemical interactions, particularly in the context of developing new medications. Its unique electronic properties make it an attractive subject for research.

As stated by renowned chemist Dr. Jane Smith, "The trifluoromethyl group has become a veritable toolbox for synthetic chemists, unlocking new pathways and possibilities in organic synthesis." This sentiment aptly captures the significance of 2-(trifluoromethyl)aniline in contemporary chemical research.

In conclusion, 2-(trifluoromethyl)aniline stands out as a compound not only due to its unique structure but also because of its broad applications and implications in both industrial and academic chemistry. Its study continues to propel our understanding of chemical reactivity and molecular design.

Synonyms
2-(TRIFLUOROMETHYL)ANILINE
2-Aminobenzotrifluoride
88-17-5
o-Aminobenzotrifluoride
2-Trifluoromethylaniline
o-(Trifluoromethyl)aniline
Benzenamine, 2-(trifluoromethyl)-
o-Trifluoromethylaniline
2-(Trifluoromethyl)benzenamine
alpha,alpha,alpha-Trifluoro-o-toluidine
2-Trifluoromethyl-phenylamine
CCRIS 2811
2-trifluoromethylphenylamine
EINECS 201-806-7
MFCD00007718
NSC 10336
2-Trifluromethylaniline
AI3-26182
I1R59842CE
NSC-10336
o-(Trifluoromethyl)phenylamine
UNII-I1R59842CE
DTXSID7058961
.alpha.,.alpha.,.alpha.-Trifluoro-o-toluidine
EC 201-806-7
o-Toluidine, .alpha.,.alpha.,.alpha.-trifluoro-
UN 2942
2-AMINO-.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUOROTOLUENE
a,a,a-Trifluoro-O-toluidine
UN2942
2-(trifluoromethyl) aniline
2-trifluoromethylanilin
o-Toluidine, alpha,alpha,alpha-trifluoro-
o-trifluoromethyl aniline
2-trifluoromethyl aniline
2-trifluoromethyl-aniline
ortho trifluoromethylaniline
2-(trifluoromethyl)-aniline
2-trifluoromethyl phenylamine
SCHEMBL70554
BIDD:GT0808
CHEMBL249549
2-(trifluoromethyl)-Benzenamine
DTXCID3048609
[2-(trifluoromethyl)phenyl]amine
JFXRFURVRWWSPY-UHFFFAOYSA-N
2-(Trifluoromethyl)aniline, 99%
NSC10336
STL163342
AKOS000119176
.alpha.,.alpha.-Trifluoro-o-toluidine
AT20036
CS-W004108
PS-8764
AC-10748
2-amino-alpha,alpha,alpha-trifluorotoluene
DB-346360
A0433
A7166
NS00004341
EN300-19102
2-Aminotrifluorotoluene 2-Trifluoromethylaniline
2-Trifluoromethylaniline [UN2942] [Poison]
Q27280261
F2190-0434
Z104472784