Interesting facts
Interesting Facts About 2-amino-4-chloro-phenol
2-amino-4-chloro-phenol, often referred to in academic and industrial circles for its unique properties, serves as an important compound in various fields of chemistry. Here are some notable insights:
- Functional Versatility: This compound acts as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals, demonstrating its versatile application in medicinal chemistry.
- Biological Importance: Research has shown that 2-amino-4-chloro-phenol exhibits antimicrobial effects, making it an interesting candidate for the development of new antibacterial agents.
- Color Reactivity: Due to the presence of both amino and chloro groups, this compound can undergo a variety of chemical reactions, leading to the formation of colored compounds that have potential applications in dye manufacturing.
- Research Potential: As scientists continue to explore the properties of 2-amino-4-chloro-phenol, there is ongoing research focusing on its environmental impact and potential applications in nanotechnology.
Quote from a researcher: "The exploration of 2-amino-4-chloro-phenol opens new avenues in both synthetic chemistry and medicinal science. Its unique reactive properties are a boon for innovation."
In conclusion, 2-amino-4-chloro-phenol not only holds significance in scientific research but also pushes the boundaries of what we can achieve with chemical synthesis in various industries.
Synonyms
2-Amino-4-chlorophenol
95-85-2
5-CHLORO-2-HYDROXYANILINE
4-Chloro-2-aminophenol
Phenol, 2-amino-4-chloro-
Fouramine PY
2-Hydroxy-5-chloroaniline
p-Chloro-o-aminophenol
2-amino-4-chloro-phenol
C.I. Oxidation Base 18
C.I. 76525
4-chloro-o-aminophenol
CCRIS 4579
UNII-2Z43LEA3DX
EINECS 202-458-9
MFCD00007694
UN2673
NSC 247814
BRN 0774859
DTXSID5024473
RODOL PY
NSC-247814
2Z43LEA3DX
DTXCID504473
EC 202-458-9
AMINO-4-CHLOROPHENOL, 2-
1-Hydroxy-2-amino-4-chlorobenzene
4-13-00-00878 (Beilstein Handbook Reference)
UN 2673
1-AMINO-2-HYDROXY-5-CHLOROBENZENE
4-chloro-2-amino phenol
2-amino-4-chlorphenol
aminochlorophenol
oAminopchlorophenol
pChlorooaminophenol
4Chloro2aminophenol
amino-4-chlorophenol
2-amino4-chlorphenol
2Hydroxy5chloroaniline
5Chloro2hydroxyaniline
Phenol, 2amino4chloro
2-amino 4-chlorophenol
2-Amino-4-Chloro phenol
2-amino -4-chloro-phenol
5-chloro-2-hydroxy-aniline
5-Chloro-2-hydroxy aniline
2-azanyl-4-chloranyl-phenol
SCHEMBL93885
O-AMINO-P-CHLOROPHENOL
CHEMBL251389
2-Amino-4-chlorophenol, 97%
4-chloro-2-amino-1-hydroxybenzene
STR04156
Tox21_201047
BBL012067
NSC247814
STK082036
AKOS000119832
CCG-302529
FC16095
4-CHLORO-2-AMINOPHENOL [INCI]
CAS-95-85-2
NCGC00091565-01
NCGC00091565-02
NCGC00091565-03
NCGC00258600-01
AC-10586
DB-057609
A0284
NS00007438
EN300-19646
2-Amino-4-chlorophenol [UN2673] [Poison]
E78988
A845483
Q27255828
F1995-0244
Z104474586
Solubility of 2-amino-4-chloro-phenol
2-amino-4-chloro-phenol, also known as p-chloroaniline, exhibits distinctive solubility characteristics that are essential for its applications in various fields. The solubility of this compound can be summarized as follows:
As with many compounds, environmental factors and pH levels can influence its solubility. In acidic conditions, the amino group can become protonated, significantly increasing solubility, while in alkaline conditions, it may revert to its non-protonated state and decrease solubility. Understanding these solubility dynamics is crucial for effective application in chemical industries.