Interesting facts
Interesting Facts about 1,2,3,4-tetrachloro-5-nitro-benzene
1,2,3,4-tetrachloro-5-nitro-benzene is a fascinating compound that showcases the complexity of aromatic chemistry. Here are some noteworthy aspects:
- Structure and Substitution: This compound is derived from a benzene ring that is substituted with multiple chlorine and nitro groups. The presence of four chlorine atoms and one nitro group greatly influences its reactivity and properties.
- Electrophilic Aromatic Substitution: The nitro group in the 5 position makes the compound highly reactive toward electrophilic substitutions. This is an essential trait that chemists leverage for various synthesis reactions.
- Environmental Impact: Due to its chlorinated nature, 1,2,3,4-tetrachloro-5-nitro-benzene can persist in the environment and may pose ecological risks. Understanding its degradation pathways is crucial for assessing its environmental footprint.
- Applications: This compound is utilized in research, particularly in the study of various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its derivatives have found applications in dyes and other chemical products.
- Health Implications: Like many chlorinated compounds, it is essential to handle 1,2,3,4-tetrachloro-5-nitro-benzene with care due to potential toxicity. The impact on human health is an area of ongoing research.
Overall, 1,2,3,4-tetrachloro-5-nitro-benzene serves as a remarkable example of the interplay between structure and function, highlighting both its utility in synthetic chemistry and the importance of environmental considerations.
Synonyms
2,3,4,5-TETRACHLORONITROBENZENE
879-39-0
1,2,3,4-Tetrachloro-5-nitrobenzene
Folosan DB-905 fumite
Benzene, 1,2,3,4-tetrachloro-5-nitro-
1-Nitro-2,3,4,5-tetrachlorobenzene
DB-905
NSC 5577
NSC 57752
2,3,4,5-Tetrachloro-1-nitrobenzene
CCRIS 5938
HSDB 4286
Benzene, 5-nitro-1,2,3,4-tetrachloro-
UNII-N2WU0K04EH
EINECS 212-906-5
N2WU0K04EH
BRN 2273256
DTXSID5026097
AI3-23025
NSC-5577
NSC-57752
DTXCID106097
MTBYTWZDRVOMBR-UHFFFAOYSA-
2,3,4,5-TETRACHLORONITROBENZENE [HSDB]
Folosan DB905 fumite
FOLSAN DB-905
1,2,3,4Tetrachloro5nitrobenzene
1Nitro2,3,4,5tetrachlorobenzene
2,3,4,5Tetrachloro1nitrobenzene
DB905
Benzene, 1,2,3,4tetrachloro5nitro
Benzene, 5nitro1,2,3,4tetrachloro
212-906-5
4-05-00-00728 (beilstein handbook reference)
inchi=1/c6hcl4no2/c7-2-1-3(11(12)13)5(9)6(10)4(2)8/h1h
mtbytwzdrvombr-uhfffaoysa-n
TCBN
Benzene,2,3,4-tetrachloro-
2,4,5-Tetrachloronitrobenzene
WLN: WNR BG CG DG EG
1,3,4-Tetrachloro-5-nitrobenzene
1-Nitro-2,4,5-tetrachlorobenzene
2,4,5-Tetrachloro-1-nitrobenzene
Benzene,2,3,4-tetrachloro-5-nitro-
MFCD00007064
1,2,3,4-tetrachloro-5-nitro-benzene
NCIOpen2_002406
MLS002152855
SCHEMBL3650611
CHEMBL1418603
NSC5577
HMS3039I09
NSC57752
Tox21_200893
AKOS015850053
2,3,4,5-tetrachloro-1-nitro-benzene
NCGC00090838-01
NCGC00090838-02
NCGC00090838-03
NCGC00258447-01
CAS-879-39-0
SMR001224479
DB-057034
CS-0157885
NS00039232
T1128
T73027
Q27284440
1,2,3,4-Tetrachloro-5-nitrobenzene, PESTANAL(R), analytical standard
Solubility of 1,2,3,4-tetrachloro-5-nitro-benzene
1,2,3,4-tetrachloro-5-nitro-benzene, with the chemical formula C6Cl4N2O2, exhibits distinct solubility characteristics that are interesting to explore.
This compound is known to be:
As stated in solubility principles, "like dissolves like." The predominance of chlorinated groups leads to a stronger attraction towards organic phase solvents than towards aqueous environments.
Overall, understanding the solubility of 1,2,3,4-tetrachloro-5-nitro-benzene is crucial for its applications in chemical synthesis and environmental assessments, where its hydrophobic character plays a significant role in its behavior and interaction with different mediums.