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Nitroaniline

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Identification
Molecular formula
C6H6N2O2
CAS number
100-01-6
IUPAC name
oxido-phenyl-phenylimino-ammonium
State
State

At room temperature, nitroaniline is generally found as a solid, existing in crystalline form.

Melting point (Celsius)
71.00
Melting point (Kelvin)
344.00
Boiling point (Celsius)
284.00
Boiling point (Kelvin)
557.00
General information
Molecular weight
138.13g/mol
Molar mass
138.1250g/mol
Density
1.4370g/cm3
Appearence

Nitroaniline is a yellow to brown crystalline solid. It can also sometimes appear as a powder. It is typically used in dyes and may have a distinct odor.

Comment on solubility

Solubility of Oxido-Phenyl-Phenylimino-Ammonium

Oxido-phenyl-phenylimino-ammonium, a fascinating chemical compound, exhibits notable solubility characteristics that can be summarized as follows:

  • Solvent Dependency: The solubility of this compound is highly dependent on the solvent used. It tends to dissolve well in polar solvents, such as water and alcohols, due to its ionic nature.
  • Temperature Influence: Increasing temperature typically enhances the solubility of oxido-phenyl-phenylimino-ammonium. As the temperature rises, the molecular interactions can weaken, allowing for easier dissolution.
  • pH Sensitivity: The solubility can also be influenced by the pH of the solution. In acidic or basic conditions, the ionization state of the compound may change, affecting its overall solubility.
  • Precipitation Risks: Reactions with certain cations or anions in solution may lead to precipitation, reducing the amount of soluble compound.

In summary, understanding the solubility of oxido-phenyl-phenylimino-ammonium involves a complex interplay of solvent choice, temperature, and environmental conditions. As stated, "The properties of solubility are not merely about dissolving; they tell a story of interaction and balance."

Interesting facts

Interesting Facts About Oxido-phenyl-phenylimino-ammonium

Oxido-phenyl-phenylimino-ammonium is a fascinating compound with a variety of unique features that make it noteworthy in the field of chemistry. Here are some interesting aspects:

  • Nature of the Compound: This compound is characterized by its unique nitrogen-oxygen framework, combining both ammonium and phenyl groups within its structure. This intricate arrangement contributes to its reactivity and potential applications.
  • Reactivity: Due to the presence of the imine group, oxido-phenyl-phenylimino-ammonium can engage in various chemical reactions. It has the potential to participate in nucleophilic and electrophilic reactions, making it valuable in synthetic chemistry.
  • Applications: Compounds like oxido-phenyl-phenylimino-ammonium have been explored in the realm of catalysis. They may serve as precursors for more complex molecules or act as catalysts themselves in organic synthesis, showcasing their versatility.
  • Research Interests: Scientists are keenly interested in understanding how the electronic properties of oxido-phenyl-phenylimino-ammonium influence its reactivity. As stated by one researcher, “The potential interactions between various functional groups within this compound open new doors for innovation in material science.”

This compound not only enriches our understanding of nitrogen chemistry but also illustrates the synergy of organic and inorganic chemistry principles. Further studies and exploration may uncover more applications, enhancing our knowledge and utilization of such unique compounds.

Synonyms
AZOXYBENZENE
495-48-7
Fenazox
Azoxybenzide
Azoxybenzol
Fentoxan
Azoxydibenzene
Azobenzene, oxide
Benzene, azoxydi-
Diphenyldiazene 1-oxide
Azossibenzene
Azoxybenzeen
Ordinary azoxybenzene
Diazene, diphenyl-, 1-oxide
Fenazox [German]
Azoxybenzeen [Dutch]
Azoxybenzol [German]
Azossibenzene [Italian]
diphenyldiazene oxide
1,2-Diphenyldiazene 1-oxide
CCRIS 5965
HSDB 2861
(phenyl-NNO-azoxy)benzene
NSC 1796
Diazene, 1,2-diphenyl-, 1-oxide
EINECS 207-802-1
UNII-X2K99TM19Q
BRN 0743984
CHEBI:51865
AI3-00476
DTXCID904555
DTXSID0024555
NSC-1796
AZOXYBENZEEN (DUTCH)
AZOXYBENZOL (GERMAN)
AZOSSIBENZENE (ITALIAN)
Benzene, azoxydi
Diphenyldiazene 1oxide
Diphenyldiazene N-oxide
AZOXYBENZENE [MI]
Diazene, diphenyl, 1oxide
AZOXYBENZENE [HSDB]
GAUZCKBSTZFWCT-YPKPFQOOSA-N
(phenyl-NNO-azoxy)benzene;diphenyldiazene oxide
207-802-1
fenazox (tn)
gauzckbstzfwct-uhfffaoysa-n
trans-azoxybenzene
cis-azoxybenzene
oxido-phenyl-phenyliminoazanium
trans-Diphenyldiazene oxide
21650-65-7
Azoxybenzene cis-form
Azoxybenzene, (E)-
Azoxybenzene, (Z)-
(E)-1,2-Diphenyldiazene 1-oxide
2CYQ7PT9SS
1,2-Diphenyldiazene oxide
Azoxybenzene cis-form [MI]
DC1P3JE72O
Azoxybenzene trans-form [MI]
CHEBI:51868
20972-43-4
NCGC00091251-01
Diazene, 1,2-diphenyl-, 1-oxide, (1E)-
Benzenamine, N-(oxidophenylimino)-, (N(Z))-
[(E)-phenyl-NNO-azoxy]benzene
CAS-495-48-7
(E)-azoxybenzene
(Z)-azoxybenzene
ZOXYBENZENE
WLN: ONR&UNR
UNII-2CYQ7PT9SS
[(E)-NNO-azoxy]benzene
[(Z)-NNO-azoxy]benzene
UNII-DC1P3JE72O
X2K99TM19Q
N,N'-Diphenyl-diazene N-oxide
(Z)-1,2-diphenyldiazene oxide
[(Z)-phenyl-NNO-azoxy]benzene
CHEMBL1442921
CHEMBL2356614
SCHEMBL14179802
CHEBI:51866
NSC1796
(Z)-1,2-diphenyldiazene 1-oxide
Tox21_111108
Tox21_201167
MFCD00019925
STL280266
(Z)-oxido-phenyl-phenylimino-ammonium
AKOS006228960
NCGC00091251-02
NCGC00258719-01
A0571
NS00000509
D88279
Q5715108
Q27122876
Q27122880