Interesting facts
Interesting Facts about 1,2,3,5-Tetrachloro-4-nitro-benzene
1,2,3,5-Tetrachloro-4-nitro-benzene is a fascinating compound that serves as an *important intermediate* in the synthesis of various chemical products. Its structure is characterized by a benzene ring that is substituted with both nitro and four chlorine atoms. Here are some intriguing aspects of this compound:
- Versatile Intermediate: Often utilized in the manufacturing of dyes, this compound’s reactivity under different conditions makes it valuable in organic synthesis.
- Environmental Considerations: The presence of chlorine atoms gives this compound notable persistence in the environment, raising considerations for its environmental impact and remediation strategies.
- Structure-Activity Relationship: The unique arrangement of chlorine and nitro groups provides a platform for chemists to study the effects of various functional groups on biological activity.
- Historical Context: Compounds like 1,2,3,5-tetrachloro-4-nitro-benzene have been instrumental in the development of chemical warfare agents, emphasizing the dual-use nature of chemical research.
As with many chlorinated aromatic compounds, it's essential to handle 1,2,3,5-tetrachloro-4-nitro-benzene with care. The potential toxicity and environmental impact highlight the need for responsible chemical management. Nevertheless, its contributions to chemical synthesis and material science continue to make it a compound of great interest in both academic and industrial chemistry.
Synonyms
1,2,3,5-Tetrachloro-4-nitrobenzene
EINECS 223-061-7
Benzene, 1,2,3,5-tetrachloro-4-nitro-
DTXSID9074987
DTXCID8039295
223-061-7
3714-62-3
SCHEMBL5921857
LOCIEHQKRSFTPA-UHFFFAOYSA-N
2,3,4,6-TETRACHLORONITROBENZENE
NS00030161
Solubility of 1,2,3,5-tetrachloro-4-nitro-benzene
1,2,3,5-tetrachloro-4-nitro-benzene, a polychlorinated aromatic compound, exhibits intriguing solubility characteristics that warrant a closer examination:
In summary, the solubility profile of 1,2,3,5-tetrachloro-4-nitro-benzene indicates a compound that is highly non-polar and prefers organic environments, aligning with its structural properties.