Interesting facts
Interesting Facts About 4-[3-(4-aminophenoxy)phenoxy]aniline
The compound 4-[3-(4-aminophenoxy)phenoxy]aniline is a fascinating molecule with notable attributes that make it a subject of interest in chemical research. Here are some key points about this compound:
- Versatile Applications: This compound is recognized for its potential use in pharmaceuticals, particularly in the development of medicinal agents. It may interact with biological systems in ways that enhance efficacy in drug formulation.
- Structural Significance: The compound's structure features a complex arrangement of aromatic rings and functional groups, which could contribute to its reactivity and properties in various chemical environments.
- Research Relevance: Scientists are exploring compounds like this one for their potential role in dye synthesis and material science. Its aniline base is prevalent in dye chemistry, which can lead to vibrant and stable colorants.
- Biological Interest: Compounds with amino and phenoxy groups are often studied for their biological activities. Researchers are investigating how these groups may influence interactions within biological systems, potentially leading to novel therapeutic strategies.
- Synthesis Insights: The synthetic pathways to create 4-[3-(4-aminophenoxy)phenoxy]aniline can involve various methodologies, including coupling reactions that highlight the importance of organic synthesis in modern chemistry.
As we dive deeper into the chemistry of this compound, it's essential to recognize the intricate balance of its structure and function. Understanding these relationships not only advances our knowledge of organic compounds but also opens doors to innovation in fields ranging from medicinal chemistry to material science.
Synonyms
1,3-Bis(4-aminophenoxy)benzene
2479-46-1
Benzenamine, 4,4'-[1,3-phenylenebis(oxy)]bis-
Resorcinol oxydianiline
4,4'-(m-Phenylenedioxy)dianiline
1,3-Phenylene-di-4-aminophenyl ether
CCRIS 6684
ANILINE, p,p'-(m-PHENYLENEDIOXY)DI-
BRN 0423316
Benzenamine, 4,4'-(1,3-phenylenebis(oxy))bis-
628-902-5
4,4'-(1,3-Phenylenedioxy)dianiline
4-[3-(4-aminophenoxy)phenoxy]aniline
RODA
1,3-Phenylenedi(4-aminophenyl ether)
Resorcinol Bis(4-aminophenyl) Ether
MFCD00039154
1,3-Bis(4-aminophenoxy)benzene(TPE-R)
MLS000719868
DTXSID8051914
SMR000304397
4,4'-(1,3-Phenylenedioxy)dianiline, 98%
4,4-(1,3-phenylenedioxy)dianiline
Maybridge3_000438
ChemDiv2_000189
Cambridge id 5128045
Oprea1_569946
SCHEMBL63594
CBDivE_002807
YSWG194
cid_17201
1,3-bis(p-aminophenoxy)benzene
CHEMBL1332684
DTXCID3030476
BDBM54332
HMS1369I13
HMS1432D20
Tox21_303941
CCG-49444
STK286018
AKOS001483293
AC-7484
CS-W012180
FB62666
4-[3-(4-azanylphenoxy)phenoxy]aniline
IDI1_011825
NCGC00245802-01
NCGC00357178-01
BS-16766
SY036265
1,3-Bis(4-aminophenoxy)benzene (TPE-R)
CAS-2479-46-1
DB-046547
[4-[3-(4-aminophenoxy)phenoxy]phenyl]amine
4,4'-[benzene-1,3-diylbis(oxy)]dianiline
4-[3-(4-Aminophenoxy)phenoxy]phenylamine #
B1680
NS00126471
F10211
SR-01000389385
SR-01000389385-1
SR-01000389385-2
BRD-K79389499-001-12-1
4,4 inverted exclamation mark -(1,3-Phenylenedioxy)dianiline
Solubility of 4-[3-(4-aminophenoxy)phenoxy]aniline
The solubility of 4-[3-(4-aminophenoxy)phenoxy]aniline, a complex organic compound, exhibits interesting characteristics influenced by its molecular structure.
Key Factors Influencing Solubility:
Generally, compounds like 4-[3-(4-aminophenoxy)phenoxy]aniline can exhibit moderate solubility in common organic solvents, but poor solubility in water due to the large non-polar portions of the molecule.
This variability makes understanding solubility essential for applications, especially in fields like pharmaceuticals where solubility affects bioavailability.
In Summary:
Understanding the solubility of 4-[3-(4-aminophenoxy)phenoxy]aniline is crucial as it plays a significant role in its usability in various applications. Consideration of polar and non-polar characteristics, alongside solvent interactions, can lead to better insights into its behavior in different environments.