Interesting facts
Interesting Facts about 4-(4-nitrophenyl)azobenzene-1,3-diol
4-(4-nitrophenyl)azobenzene-1,3-diol, commonly referred to in academic literature as an azo compound, has sparked considerable interest in the field of chemical research due to its fascinating properties and applications. Here are some engaging facts about this compound:
- Azo Compounds: Azo compounds, characterized by the presence of (-N=N-) group, are widely studied for their chromogenic properties. This makes them significant in various fields including dyes, sensors, and photonic devices.
- Nitrophenyl Group: The incorporation of a nitrophenyl group into this molecule enhances its electronic properties, which can be advantageous for applications in organic electronics and photonic materials.
- Dual Functionality: The presence of both an azo group and hydroxyl groups gives this compound unique properties, making it an excellent candidate for biological assays as well as catalytic applications.
- Environmental Significance: As industries increasingly consider environmental impact, azo compounds like this one are scrutinized for their potential toxicity. Understanding their behavior and degradation pathways in biological systems is crucial for minimizing ecological risks.
- Research Applications: This compound finds applications in research aimed at exploring molecular interactions and photochemical reactions, providing valuable insights into molecular dynamics.
To summarize, 4-(4-nitrophenyl)azobenzene-1,3-diol is not just a chemical entity but a gateway to exploring advanced concepts in material science and environmental chemistry. Its unique structural features make it a worthy subject for continued investigation and application.
Synonyms
4-(4-Nitrophenylazo)resorcinol
74-39-5
Magneson
Magneson I
p-Diazoviolet
p-Nitrophenylazoresorcinol
Magnezon I
p-Nitrobenzeneazoresorcinol
4-((4-Nitrophenyl)diazenyl)benzene-1,3-diol
Azoviolet
p-Diazviolet
4-(p-Nitrophenylazo)resorcinol
4-(4-Nitrophenyl)azoresorcinol
AZO VIOLET
2,4-Dihydroxy-4'-nitroazobenzene
1,3-Benzenediol, 4-[(4-nitrophenyl)azo]-
4-(4-nitro-phenylazo)-resorcinol
NSC 3914
4-((4-Nitrophenyl)azo)-1,3-benzenediol
p-nitro-4-azoresorcin
Magneson centn
YND5ZT5BS3
EINECS 200-808-5
4-[(4-nitrophenyl)diazenyl]benzene-1,3-diol
111650-65-8
AI3-09041
1,3-Benzenediol, 4-((4-nitrophenyl)azo)-
MAGNESON [MI]
NSC-3914
MFCD00007310
Resorcinol, 4-((p-nitrophenyl)azo)-
1,3-Benzenediol, 4-(2-(4-nitrophenyl)diazenyl)-
1,3-dihydroxy-4-(4-nitrophenylazo)benzene
MLS000530152
CHEBI:66930
DTXSID30861621
4-(2-(4-nitrophenyl)diazenyl)-1,3-benzenediol
4-[(E)-(4-nitrophenyl)diazenyl]benzene-1,3-diol
Diazo Violet; Magneson; Magneson I
Resorcinol, 4-[(p-nitrophenyl)azo]-
SMR000135130
4-[(4-Nitrophenyl)azo]-1,3-benzenediol
4-[(4-nitrophenyl)diazenyl]-1,3-benzenediol
(E)-4-((4-nitrophenyl)diazenyl)benzene-1,3-diol
1,3-Benzenediol, 4-[2-(4-nitrophenyl)diazenyl]-
4-((E)-(4-nitrophenyl)diazenyl)benzene-1,3-diol
UNII-YND5ZT5BS3
pDiazoviolet
pDiazviolet
4(p-Nitrophenylazo)resorcinol
Magneson?
C12H9N3O4
pNitrophenylazoresorcinol
pNitrobenzeneazoresorcinol
4(pNitrophenylazo)resorcinol
NCIOpen2_004077
4(4Nitrophenyl)azoresorcinol
2,4Dihydroxy4'nitroazobenzene
SCHEMBL1289510
4-(p-Nitrobenzeneazo)resorcinol
4-Nitrophenylazo-4'-resorcinol
4-(4-Nirophenylazo)-resorcinol
CHEMBL1604790
BDBM57169
cid_5717413
1, 4-[(4-nitrophenyl)azo]-
DTXCID00810520
NSC3914
NGPGYVQZGRJHFJ-BUHFOSPRSA-N
NGPGYVQZGRJHFJ-UHFFFAOYSA-N
HMS2388J09
4-(para-Nitrophenylazo)-resorcinol
HY-D0228
4((4Nitrophenyl)azo)1,3benzenediol
(4E)-3-hydroxy-4-[(4-nitrophenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one
AKOS015902695
AKOS024306973
1,3Benzenediol, 4((4nitrophenyl)azo)
4-(4-Nitrophenylazo)resorcinol, 90+%
NCGC00245704-01
AC-16671
AS-75627
DB-055872
CS-0010139
N0135
NS00041178
4-(4-Nitrophenylazo)resorcinol, p.a., 95%
H11863
4-((4-Nitrophenyl);diazenyl);benzene-1,3-diol
4-[(4-Nitrophenyl)diazenyl]-1,3-benzenediol #
A865908
SR-01000196070
4-(4-Nitrophenylazo)resorcinol, Dye content 90 %
Q4676694
SR-01000196070-1
(4E)-3-hydroxy-4-[(4-nitrophenyl)hydrazinylidene]-1-cyclohexa-2,5-dienone
(4E)-3-hydroxy-4-[(4-nitrophenyl)hydrazono]cyclohexa-2,5-dien-1-one
(4E)-4-[(4-nitrophenyl)hydrazinylidene]-3-oxidanyl-cyclohexa-2,5-dien-1-one
3-HYDROXY-4-[2-(4-NITROPHENYL)HYDRAZIN-1-YLIDENE]CYCLOHEXA-2,5-DIEN-1-ONE
Solubility of 4-(4-nitrophenyl)azobenzene-1,3-diol (C12H9N3O3)
The solubility of the compound 4-(4-nitrophenyl)azobenzene-1,3-diol is influenced by its molecular structure, functional groups, and polarity. Here are some key points to consider:
Overall, while 4-(4-nitrophenyl)azobenzene-1,3-diol exhibits some degree of solubility in polar solvents, it is not highly soluble in water due to its structural characteristics. As such, careful selection of solvents is crucial for experiments and applications involving this compound.