Interesting facts
Interesting Facts about 1,3,5-Trichloro-2-nitro-benzene
1,3,5-Trichloro-2-nitro-benzene, often abbreviated as TCNB, is a fascinating organic compound with several noteworthy characteristics and applications. Here are some engaging facts about this compound:
- Chemical Structure: TCNB features a unique aromatic ring structure, containing both nitro (-NO2) and chloro (-Cl) functional groups. The presence of three chlorine atoms on the benzene ring significantly influences its chemical reactivity.
- Use in Research: TCNB is extensively utilized in chemical research, particularly for studying the reactivity of halogenated compounds. Researchers often delve into the mechanisms of nucleophilic substitution reactions involving such halogenated aromatic compounds.
- Environmental Impact: Due to its halogenated nature, TCNB raises concerns regarding environmental toxicity. Its persistence in the environment can lead to adverse ecological effects, highlighting the importance of monitoring and regulation.
- Analytical Applications: TCNB acts as an important compound in analytical chemistry. It is often employed as a standard in qualitative analysis to help identify the presence of similar halogenated compounds.
- Structure-Activity Relationships: TCNB serves as a model compound to elucidate structure-activity relationships (SAR) in toxicology studies. Understanding how modifications to the structure influence biological activity is crucial in the field of medicinal chemistry.
In conclusion, 1,3,5-trichloro-2-nitro-benzene is not just a chemical entity; it forms a bridge between theoretical and applied chemistry. Its relevance in research and its impact on the environment make it a compound worthy of attention among scientists and students alike.
Synonyms
2,4,6-Trichloronitrobenzene
18708-70-8
1,3,5-Trichloro-2-nitrobenzene
Benzene, 1,3,5-trichloro-2-nitro-
2,4,6-Trichloro-1-nitrobenzene
UNII-T00KP6CT7K
EINECS 242-518-1
T00KP6CT7K
NSC 10244
DTXSID0026204
NSC-10244
DTXCID606204
1-Nitro-2,4,6-trichlorobenzene
1-Nitro-2,4-6-trichloro benzene
TRICHLORONITROBENZENE, 2,4,6-
AEBJDOTVYMITIA-UHFFFAOYSA-N
2,4,6-Trichloronitro Benzene
MFCD00014690
1,3,5-tris(chloranyl)-2-nitro-benzene
1,3,5-trichloro-2-nitro-benzene
NSC10244
Benzene,1,3,5-trichloro-2-nitro-
2,6-Trichloronitrobenzene
1,3,5-trichloronitrobenzene
MLS002152859
SCHEMBL954217
2,4,6-trichloro nitrobenzene
1,5-Trichloro-2-nitrobenzene
2,6-Trichloro-1-nitrobenzene
CHEMBL1333420
Benzene,3,5-trichloro-2-nitro-
Tox21_200687
AKOS015833795
NCGC00090831-01
NCGC00090831-02
NCGC00258241-01
LS-13112
SMR001224483
SY106078
CAS-18708-70-8
DB-044630
CS-0196918
NS00026115
ST50826885
T0388
EN300-7867967
A813114
Q27289491
1,3,5-Trichloro-2-nitrobenzene, technical, ~85% (HPLC)
Solubility of 1,3,5-Trichloro-2-nitro-benzene
1,3,5-Trichloro-2-nitro-benzene is a chemical compound that exhibits unique solubility characteristics due to its structural composition. Understanding its solubility can be approached through several important points:
To summarize, while 1,3,5-trichloro-2-nitro-benzene is primarily insoluble in water, it can readily dissolve in non-polar organic solvents. This feature highlights the importance of solvent selection in applications involving this compound. As the saying goes, "like dissolves like," which rings true in the case of this aromatic compound.