Interesting facts
Interesting Facts about 3-(Trifluoromethyl)phenol
3-(Trifluoromethyl)phenol, also known as a substituted phenolic compound, has garnered significant interest in various fields due to its unique properties and potential applications. Here are some captivating insights:
- **Chemical Structure**: The presence of the trifluoromethyl group (-CF3) significantly enhances the compound's lipophilicity, making it highly relevant in medicinal chemistry.
- **Biological Activity**: This compound exhibits notable antibacterial activity, which opens avenues for its use in pharmaceuticals. Studies have indicated that it may inhibit the growth of certain pathogens.
- **Industrial Use**: Beyond its biological implications, 3-(Trifluoromethyl)phenol is commonly utilized as a building block in the synthesis of agrochemicals and fluorinated materials.
- **Research Interest**: Ongoing research focuses on its role in organic electronics and materials science, particularly in the development of new polymers and coatings.
- **Fluorine Chemistry**: The trifluoromethyl group is a highly electronegative substituent, influencing the reactivity of the compound, making it a subject of interest for chemists studying fluorine chemistry.
As a fascinating compound, 3-(Trifluoromethyl)phenol exemplifies the power of fluorination in altering chemical properties, paving the way for innovative applications across chemistry and material science.
Synonyms
3-(Trifluoromethyl)phenol
98-17-9
3-Trifluoromethylphenol
3-Hydroxybenzotrifluoride
m-Hydroxybenzotrifluoride
m-trifluoromethylphenol
Phenol, 3-(trifluoromethyl)-
m-(Trifluoromethyl)phenol
alpha,alpha,alpha-Trifluoro-m-cresol
a,a,a-trifluoro-m-cresol
5-TRIFLUOROMETHYLPHENOL
NSC 9884
EINECS 202-645-5
3-Trifluoromethyl-phenol
MFCD00002299
m-CRESOL, alpha,alpha,alpha-TRIFLUORO-
DTXSID7052658
EC 202-645-5
NSC-9884
m-Cresol, .alpha.,.alpha.,.alpha.-trifluoro-
3-Hydroxy-alpha,alpha,alpha-trifluorotoluene
ALPHA,A,A-Trifluoro-m-cresol
3-trifluoromethylplienol
m-trifluoromethyl-phenol
3-trifluoromethyl phenol
meta-trifluoromethylphenol
3-(triluoromethyl)phenol
3-hydroxy benzotrifluoride
3-hydroxy-benzotrifluoride
m-CF3C6H4OH
meta-trifluoromethyl phenol
3-(trifluoromethyl) phenol
phenol, 3-trifluoromethyl-
R2R9N38UDY
SCHEMBL40389
CHEMBL57877
DTXCID8031231
NSC9884
3-(Trifluoromethyl)phenol, 99%
CHEBI:195128
BDBM108237
3-(1,1,1-trifluoromethyl)phenol
.alpha.,.alpha.-Trifluoro-m-cresol
BBL009723
STL141088
alpha,alpha,alpha,-trifluoro-m-cresol
AKOS000119745
alpha, alpha, alpha-trifluoro-m-cresol
CS-W010869
FH33135
PS-8757
AC-10892
M‐trifluoromethylphenol (Hit 5)
DB-028582
.alpha.,.alpha.,.alpha.-Trifluoro-m-cresol
NS00010084
T0436
EN300-20070
D70669
F0001-2315
Z104476676
1-TRIFLUOROMETHYL,3-HYDROXY-BENZENE (3-HYDROXI-TOLUENE,ALPHA,ALPHA,ALPHA-TRIFLUORO)
1-TRIFLUOROMETHYL,3-HYDROXY-BENZENE (3-HYDROXI-TOLUENE,ALPHA,ALPHA,ALPHA-TRIFLUORO)
m-Hydroxybenzotrifluoride ; 3-Hydroxybenzotrifluoride ; 3-(Trifluoromethyl)phenol ; alpha,alpha,alpha-Trifluoro-m-cresol
m-Hydroxybenzotrifluoride; 3-Hydroxybenzotrifluoride; 3-(Trifluoromethyl)phenol; alpha,alpha,alpha-Trifluoro-m-cresol
Solubility of 3-(trifluoromethyl)phenol
3-(trifluoromethyl)phenol, a derivative of phenolic compounds, exhibits unique solubility characteristics due to the influence of its trifluoromethyl group.
In general, the solubility of 3-(trifluoromethyl)phenol can be summarized as follows:
As with many organic compounds containing fluorinated groups, their solubility properties can be quite distinct. Thus, it is often observed that:
In conclusion, understanding the solubility of 3-(trifluoromethyl)phenol is crucial for applications in synthesis and chemical reactions, reinforcing the adage that “the solubility of a compound often dictates its reactivity.”