Interesting facts
Interesting Facts about 4-[(2-chloroacetyl)amino]phenyl]arsonic acid
4-[(2-chloroacetyl)amino]phenyl]arsonic acid, commonly known in scientific circles, has a rich history in both biochemical research and application. This compound is particularly notable for its role in various fields, ranging from medicinal chemistry to agricultural sciences. Here are some fascinating insights:
- Historical Significance: This compound, often associated with veterinary medicine, reflects the evolving landscape of drug development over the decades. Its use in the treatment of infections in livestock has been a topic of various studies.
- Mechanism of Action: 4-[(2-chloroacetyl)amino]phenyl]arsonic acid is believed to function by disrupting biochemical pathways in microbial organisms, showcasing how chemical modifications can enhance efficacy against pathogens.
- Structural Features: The presence of both chloroacetyl and arsonic functional groups in this compound provides it with unique reactivity. These groups allow for specific interactions that can lead to significant biological effects.
- Research Applications: Beyond its medicinal use, compounds like this one are often employed in research laboratories to investigate mechanisms of drug resistance and the synthesis of new therapeutic agents.
- Controversial Aspects: As an organoarsenic compound, it sparks discussions regarding environmental implications and the safety of arsenic-containing compounds in agriculture, highlighting the need for responsible usage.
In conclusion, 4-[(2-chloroacetyl)amino]phenyl]arsonic acid stands as an example of the intricate relationship between chemistry and real-world applications. Its history, mechanisms, and implications in various fields underline its significance in scientific discovery.
Synonyms
5425-62-7
NSC 12629
EINECS 226-569-7
NSC 43640
BRN 2981394
(4-((Chloroacetyl)amino)phenyl)arsonic acid
ARSONIC ACID, (4-((CHLOROACETYL)AMINO)PHENYL)-
Acide monochloroacetamido-4 benzene arsonique [French]
Acide monochloroacetamido-4 benzene arsonique
DTXSID20202605
Arsonic acid, [4-[(chloroacetyl)amino]phenyl]-
DTXCID10125096
3-16-00-01110 (beilstein handbook reference)
4-(2-Chloroacetamido)phenylarsonic acid
ANTINEOPLASTIC-12629
ANTINEOPLASTIC-43640
BWPMHDNLIGQVLN-UHFFFAOYSA-N
NSC12629
NSC43640
NSC-12629
NSC-43640
NS00080930
Solubility of [4-[(2-chloroacetyl)amino]phenyl]arsonic Acid
[4-[(2-chloroacetyl)amino]phenyl]arsonic acid, a compound with complex functional groups, exhibits distinctive solubility characteristics that are essential for understanding its behavior in various environments. Its solubility can be influenced by several factors:
In summary, while [4-[(2-chloroacetyl)amino]phenyl]arsonic acid may dissolve well in polar solvents, the extent of its solubility can vary significantly under different conditions. Understanding these solubility dynamics is crucial for applications in pharmaceuticals and environmental chemistry.