Interesting facts
Interesting Facts about 1,2,4,5-Tetrachloro-3-methoxy-6-nitro-benzene
1,2,4,5-Tetrachloro-3-methoxy-6-nitro-benzene, often referred to in research as a halogenated aromatic compound, is a fascinating subject of study due to its unique structural features and diverse applications. Here are some notable facts:
- Halogen Bonding: The presence of four chlorine atoms in its structure not only enhances its stability but also contributes to its reactivity. Halogenated compounds are known for their ability to engage in halogen bonding, which can influence molecular interactions significantly.
- Environmental Impact: Compounds like this one are often scrutinized for their persistence in the environment. Chlorinated aromatic compounds can pose environmental risks and considerations regarding their degradation and bioaccumulation.
- Applications in Synthesis: This compound serves as a valuable intermediate in the synthesis of other chemical products. Its structure allows it to participate in various chemical reactions, making it useful in creating complex organic molecules.
- Biological Activity: Some halogenated aromatic compounds exhibit interesting biological activities. As such, studying their mechanisms can provide insights into drug design and development, particularly in the context of >pharmaceutical research.
- Colorimetric Indicators: The nitro group (-NO2) present in the molecule imparts specific optical properties, which can be harnessed for colorimetric assays in various analytical methods.
In summary, 1,2,4,5-tetrachloro-3-methoxy-6-nitro-benzene offers a unique combination of stability, reactivity, and potential applications that make it a captivating subject of study in both synthetic and environmental chemistry. Its role in research not only enhances our understanding of halogenated compounds but also emphasizes the importance of studying the effects of human-made compounds on ecological systems.
Synonyms
2,3,5,6-TETRACHLORO-4-NITROANISOLE
2438-88-2
1,2,4,5-Tetrachloro-3-methoxy-6-nitrobenzene
Tetrachloronitroanisole
NCI-C03032
ENT 22,335
CCRIS 580
4-Nitro-2,3,5,6-tetrachloranisole
NSC 407047
HSDB 4119
UNII-AOX0D94LLR
AOX0D94LLR
Anisole, 2,3,5,6-tetrachloro-4-nitro-
Benzene, 1,2,4,5-tetrachloro-3-methoxy-6-nitro-
BRN 2382408
AI3-22335
NSC-407047
DTXSID2021313
TETRACHLORO-4-NITROANISOLE
ENT-22335
TETRACHLORO-4-NITROANISOLE, 2,3,5,6-
2,3,5,6-TETRACHLORO-4-NITROANISOLE [HSDB]
DTXCID201313
4Nitro2,3,5,6tetrachloranisole
Anisole, 2,3,5,6tetrachloro4nitro
1,2,4,5Tetrachloro3methoxy6nitrobenzene
Benzene, 1,2,4,5tetrachloro3methoxy6nitro
Benzene, 1,2,4,5-tetrachloro-3-methoxy-6-nitro-(9CI)
3-06-00-00842 (beilstein handbook reference)
TCNA
CHEMBL405522
SCHEMBL10984978
BGPPUXMKKQMWLV-UHFFFAOYSA-N
4-Nitro-2,5,6-tetrachloranisole
2,5,6-Tetrachloro-4-nitroanisole
WLN: WNR BG CG EG FG DO1
NSC407047
Anisole,3,5,6-tetrachloro-4-nitro-
NS00120385
Benzene,2,4,5-tetrachloro-3-methoxy-6-nitro-
Q27274042
Solubility of 1,2,4,5-Tetrachloro-3-methoxy-6-nitro-benzene
1,2,4,5-Tetrachloro-3-methoxy-6-nitro-benzene, often abbreviated for convenience, presents interesting solubility characteristics due to its complex molecular structure. Understanding the solubility of this compound is crucial in various chemical applications. Here are some key points regarding its solubility:
The unique juxtaposition of functional groups within the molecular design of 1,2,4,5-tetrachloro-3-methoxy-6-nitro-benzene results in its specific solubility behavior, making it a noteworthy compound for study within organic chemistry.