Interesting facts
Interesting Facts about 4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid
4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid, often abbreviated as HAPA, is a unique organoarsenic compound with a variety of intriguing properties and applications. Here are some noteworthy aspects of this fascinating compound:
- Historical Usage: This compound has been studied for its potential use as a therapeutic agent, particularly in the treatment of parasitic infections and certain types of cancer due to its ability to interact with biological systems.
- Biological Significance: Organosilicon compounds, such as HAPA, often exhibit interesting biological activities. HAPA’s structure allows it to interact with specific enzymes, making it a target for research into novel pharmaceutical applications.
- Toxicity Research: Scientists are actively investigating the toxicity and environmental impact of arsenic-containing compounds. Understanding HAPA can provide insights into the potential risks and safe handling procedures associated with organoarsenic species.
- Analytical Chemistry: HAPA has been utilized in analytical chemistry as a standard substance in the calibration of instruments and methods designed to detect other arsenic compounds in various matrices.
- Innovative Applications: Ongoing research is exploring the use of HAPA in developing new materials and techniques across fields such as biochemistry, environmental science, and pharmaceuticals.
In summary, 4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid exemplifies the complexity and versatility of organoarsenic compounds. Its varied applications highlight the intersection of chemistry, biology, and environmental science, making it a compound worth further exploration. As the research continues to evolve, we may uncover even more applications and implications of HAPA that can benefit both science and society.
Synonyms
Glycarsamide
144-87-6
4-(Glycolloylamino)phenylarsonic acid
Astryl
N-Glycolylarsanilic acid
[4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid
N-Glycoloylarsanilic acid
3ACA67L6DG
Arsanilic acid, N-glycoloyl-
p-Glycolylaminophenylarsinic acid
NSC-221701
NSC163966
[4-[(HYDROXYACETYL)AMINO]PHENYL]ARSONIC ACID
NSC-163966
(4-((HYDROXYACETYL)AMINO)PHENYL)ARSONIC ACID
UNII-3ACA67L6DG
EINECS 205-643-2
GLYCARSAMIDE [MI]
NCIStruc1_001581
NCIStruc2_001935
SCHEMBL225259
CHEMBL1741842
DTXSID40162595
p-Glycoloylaminophenylarsinic acid
p-Glycoloylaminophenylarsonic acid
p-Glycolylaminobenzenearsonic acid
p-Glycoloylaminobenzenearsonic acid
QABXFDAPQQVMKL-UHFFFAOYSA-N
p-Hydroxyacetamidophenylarsonic acid
4-(glycoloylamino)phenylarsonic acid
CCG-36631
MFCD00068960
NCGC00014459
NCI163966
NSC221701
AKOS023506036
NSC 221701
NCGC00014459-02
NCGC00097564-01
NCI60_001246
Arsonic acid, [4-[(hydroxyacetyl)amino]phenyl]-
Q27256967
Solubility of [4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid
[4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid, with its complex structure, exhibits notable solubility characteristics. This compound can be analyzed based on several solubility factors:
As a result, it can be said that [4-[(2-hydroxyacetyl)amino]phenyl]arsonic acid is relatively soluble in polar solvents, particularly in an aqueous environment, influenced by pH and temperature. This solubility profile can play a vital role in its application and handling in various chemical processes.