Interesting facts
Interesting Facts about 1,2,3,5-Tetrachloro-4-methoxy-benzene
1,2,3,5-Tetrachloro-4-methoxy-benzene, often known by its common name, makes for a compelling subject of study in the field of organic chemistry. This compound is noteworthy for several reasons:
- Structure and Functinality: This compound features a complex structure characterized by a benzene ring that is heavily substituted with chlorine atoms and a methoxy group. The presence of both electron-withdrawing (chlorine) and electron-donating (methoxy) groups leads to intriguing electronic properties.
- Applications: Compounds like 1,2,3,5-tetrachloro-4-methoxy-benzene are often discussed in the context of their use in the production of pesticides and herbicides. Understanding such compounds allows chemists to develop more effective agrochemicals for agricultural use.
- Environmental Impact: The chlorinated nature of this compound raises important discussions about environmental chemistry. Chlorinated organic compounds can be persistent in the environment and are subject to studies focusing on their degradation and toxicology.
- Reactivity: The chlorine atoms in this compound make it highly reactive, participating in various substitution and elimination reactions. This reactivity can be exploited in organic synthesis to create even more complex molecules.
- Symbol of Complexity: Compounds like this serve as a prime example of how small modifications in molecular structure can result in vastly different chemical behaviors and properties. This idea is crucial for students learning about structure-activity relationships in medicinal chemistry.
As one explores the intricacies of 1,2,3,5-tetrachloro-4-methoxy-benzene, it becomes clear that the study of such compounds is vital for advancing our knowledge in both organic synthesis and environmental chemistry. Researchers often say, "Chemistry is not just a subject; it’s a way of thinking about the world around us." This sentiment resonates with the importance of understanding compounds like this in addressing real-world challenges.
Synonyms
2,3,4,6-TETRACHLOROANISOLE
938-22-7
Benzene, 1,2,3,5-tetrachloro-4-methoxy-
Anisole, 2,3,4,6-tetrachloro-
2,4,5,6-Tetrachloroanisole
UNII-SJ2G6F3F2Y
SJ2G6F3F2Y
DTXSID80239654
DTXCID30162145
itxdbglyysjnpk-uhfffaoysa-n
1,2,3,5-Tetrachloro-4-methoxybenzene
1,2,3,5-Tetrachloro-4-methoxy-Benzene
methyl 2,3,4,6-tetrachlorophenyl ether
Anisole, 2,3,4,6-tetrachloro- (7CI,8CI); 1,2,3,5-Tetrachloro-4-methoxybenzene; 2,3,4,6-Tetrachloroanisole; 2,4,5,6-Tetrachloroanisole
SCHEMBL481060
2,3,4,6-Tetrachloro-Anisole
CHEBI:178118
BS-52421
FT146474
1,2,3,5-Tetrachloro-4-methoxybenzene #
NS00122366
C13371
AH-034/32830058
Q27289235
2,3,4,6-Tetrachloroanisole 100 microg/mL in Hexane/Acetone 9:1
Solubility of 1,2,3,5-tetrachloro-4-methoxy-benzene
1,2,3,5-tetrachloro-4-methoxy-benzene, also known as chlorinated aromatic compound, exhibits interesting solubility characteristics. This compound is primarily non-polar due to the presence of multiple chlorine atoms and the methoxy group, which affects its ability to interact with solvent molecules.
The solubility of this compound can be summarized as follows:
In general, the compound's solubility can be affected by factors such as temperature and the presence of other chemicals in the solution. It’s important to remember that as an aromatic compound, 1,2,3,5-tetrachloro-4-methoxy-benzene may participate in various interactions, thus influencing its solubility in different environments. The statement that "like dissolves like" holds true here, making the solubility a vivid reflection of its molecular structure.