Interesting facts
Interesting Facts About 1-Bromo-3-(Trifluoromethyl)benzene
1-Bromo-3-(trifluoromethyl)benzene, often referred to in the scientific community for its unique properties, is a compelling compound that offers a wealth of insights in both organic chemistry and material science. Here are some noteworthy points about this fascinating compound:
- Structure and Substitution: The compound features a benzene ring substituted at the 1-position by a bromo group (Br) and at the 3-position by a trifluoromethyl group (–CF3). The positioning of these substituents plays a critical role in influencing the compound's reactivity and properties.
- Reactivity: The presence of the trifluoromethyl group significantly alters the electron density of the aromatic ring, making it more resistant to electrophilic substitutions. This characteristic is particularly useful in synthetic organic chemistry for creating derivatives with selective functionalities.
- Applications: Compounds like 1-Bromo-3-(trifluoromethyl)benzene are of interest in agrochemicals and pharmaceuticals. They act as intermediates in the production of various biologically active compounds and can be crucial in creating novel materials.
- Physical Properties: With its unique electronegative trifluoromethyl group, this compound has distinct physical properties when compared to other halogenated benzenes. These properties can influence its behavior in solvent systems, making it invaluable in understanding solvent interactions.
- Environmental Considerations: As with other halogenated compounds, the environmental impact and degradation of 1-bromo-3-(trifluoromethyl)benzene warrant careful consideration, as they can pose risks to ecosystems.
In conclusion, 1-bromo-3-(trifluoromethyl)benzene serves not only as a subject of study for its intrinsic chemical properties but also as a gateway into broader discussions about chemical reactivity, synthesis, and environmental health. As scientists continue to explore its potential, this compound stands as an example of the complexity and utility found within organic chemistry.
Synonyms
3-Bromobenzotrifluoride
401-78-5
1-Bromo-3-(trifluoromethyl)benzene
m-Bromobenzotrifluoride
3-(Trifluoromethyl)bromobenzene
Benzene, 1-bromo-3-(trifluoromethyl)-
3-Bromobenzyltrifluoride
3-Bromotrifluoromethylbenzene
3-Brombenzotrifluorid
3-(Trifluoromethyl)phenyl bromide
m-(Trifluoromethyl)bromobenzene
3-Bromo-alpha,alpha,alpha-trifluorotoluene
m-(Trifluoromethyl)phenyl bromide
m-Bromo(trifluoromethyl)benzene
m-Bromo-alpha,alpha,alpha-trifluorotoluene
NSC 9468
MFCD00000380
3-Brombenzotrifluorid [Czech]
EINECS 206-932-6
BRN 1449557
Toluene, alpha,alpha,alpha-trifluoro-3-bromo-
TOLUENE, m-BROMO-alpha,alpha,alpha-TRIFLUORO-
DTXSID1059947
1-bromo-3-trifluoromethylbenzene
NSC-9468
Toluene, m-bromo-.alpha.,.alpha.,.alpha.-trifluoro-
3-BROMOTRIFLUOROTOLUENE
1-Bromo-3-trifluoromethyl-benzene
3-bromo-1-(trifluoromethyl)benzene
3-bromo benzotrifluoride
3-bromo-benzotrifluoride
meta-bromobenzotrifluoride
WLN: FXFFR CE
m-bromotrifluoromethylbenzene
SCHEMBL4661
m-Trifluoromethylbromobenzene
3-Trifluoromethylbromobenzene
3-bromo-trifluoromethylbenzene
3-trifluoromethyl-bromobenzene
m-trifluoromethylphenyl bromide
3-trifluoromethylphenyl bromide
3-Bromobenzotrifluoride, 99%
9A2GF99MK4
DTXCID6039714
2-bromo-4-trifluoromethylbenzene
3-(trifluoromethyl)-bromobenzene
3-Bromo-5-trifluoromethylbenzene
3-trifluoromethyl-1-bromobenzene
NSC9468
AKOS000121505
AC-1780
CS-W019942
FB64582
m-Bromo-.alpha.,.alpha.-trifluorotoluene
3-bromo-I+/-,I+/-,I+/--trifluorotoluene
B0664
NS00043142
Toluene,.alpha.,.alpha.-trifluoro-3-bromo-
EN300-21162
m-Bromotrifluorotoluene; m-Bromobenzotrifluoride
m-Bromo-.alpha.,.alpha.,.alpha.-trifluorotoluene
Toluene, .alpha.,.alpha.,.alpha.-trifluoro-3-bromo-
F0001-1129
1-Bromo-3-(trifluoromethyl)benzene, 3-Bromo-alpha,alpha,alpha-trifluorotoluene
Solubility of 1-bromo-3-(trifluoromethyl)benzene
The solubility of 1-bromo-3-(trifluoromethyl)benzene, a compound with the chemical formula C8H5BrF3, exhibits interesting characteristics due to its structural components. Here are some key points regarding its solubility:
In summary, while 1-bromo-3-(trifluoromethyl)benzene is quite soluble in nonpolar solvents, its polar solubility is significantly challenged, making it a compound that is best suited for organic reactions rather than aqueous environments. As the saying goes, "like dissolves like," and this principle plays a crucial role in determining the solubility behaviors of this compound.