Interesting facts
Interesting Facts About 1-Nitro-4-(trifluoromethyl)benzene
1-Nitro-4-(trifluoromethyl)benzene, often referred to as a derivative of nitrobenzene, is a fascinating compound that showcases the intriguing world of organic chemistry. It carries significant implications in both research and industrial applications.
Chemical Significance
- Substituted Aromatic Compound: This compound is notable for its substitution pattern on the benzene ring, where a nitro group and a trifluoromethyl group are both present, influencing its reactivity and electronic properties.
- Electrophilic Aromatic Substitution: The presence of the nitro group makes this compound a good candidate for further substitution reactions, as it is a strong electron-withdrawing group that can enhance electrophilicity.
Applications
- Pharmaceutical Synthesis: Compounds like 1-nitro-4-(trifluoromethyl)benzene are often utilized as intermediates in the synthesis of various pharmaceuticals and agrochemicals.
- Material Science: This compound may be explored for potential applications in creating advanced materials due to the unique properties conferred by the trifluoromethyl group, which can provide thermal stability and chemical resistance.
Properties and Behaviors
When studying 1-nitro-4-(trifluoromethyl)benzene, one can observe:
- Hydrophobic Nature: The trifluoromethyl group contributes to its low solubility in water, making it relevant for research in environmental chemistry, particularly in assessing the behavior of contaminants.
- Reactivity Patterns: The unique combination of functional groups allows chemists to predict and manipulate its reactivity, guiding pathways for designing new chemical entities.
In summary, 1-nitro-4-(trifluoromethyl)benzene is more than just a simple compound; it is a gateway to exploring the complex interplay of substituents within organic chemistry. As scientists continue to delve into its properties and potential applications, it stands as a testament to the innovative spirit of the field.
Synonyms
4-Nitrobenzotrifluoride
402-54-0
1-Nitro-4-(trifluoromethyl)benzene
p-Nitrobenzotrifluoride
Benzene, 1-nitro-4-(trifluoromethyl)-
4-(TRIFLUOROMETHYL)NITROBENZENE
4-Nitro-alpha,alpha,alpha-trifluorotoluene
4-NITRO-A,A,A-TRIFLUOROTOLUENE
p-Nitro(trifluoromethyl)benzene
NSC 159121
4-nitro-1-(trifluoromethyl)benzene
NSC-159121
ALPHA,ALPHA,ALPHA-TRIFLUORO-P-NITROTOLUENE
4-Nitro-.alpha.,.alpha.,.alpha.-trifluorotoluene
MFCD00007358
p-nitro-Trifluoromethylphenol
EINECS 206-948-3
4-nitrobenzotrifluorid
4-(TRIFLUOROMETHYL)-1-NITROBENZENE
N47TT2JQ3Y
SCHEMBL439543
4-Nitrobenzotrifluoride, 98%
DTXSID0075281
1-Nitro-4-trifluoromethyl-benzene
1-nitro-4-(trifluoromethyl)-benzene
NSC159121
AKOS015889713
P-(TRIFLUOROMETHYL)NITROBENZENE
AC-4147
CS-W015852
FN97995
AS-16062
A1677
N0902
NS00043263
Toluene, 4-nitro-.alpha.,.alpha.,.alpha.-trifluoro-
TOLUENE, ALPHA,ALPHA,ALPHA-TRIFLUORO-P-NITRO-
Z56762338
4-Nitro-alpha,alpha,alpha-trifluorotoluene;4-(trifluoromethyl)nitrobenzene
Solubility of 1-nitro-4-(trifluoromethyl)benzene
1-nitro-4-(trifluoromethyl)benzene, with its unique molecular structure, exhibits particular solubility characteristics that are influenced by its functional groups. This compound is predominantly non-polar due to the significant presence of the trifluoromethyl group, which imparts hydrophobic properties.
Here are some key points regarding its solubility:
As a result, while 1-nitro-4-(trifluoromethyl)benzene may not readily dissolve in water, its compatibility with various organic solvents opens up avenues for diverse applications in chemical synthesis and material science.