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N'-(4-nitrosophenyl)benzohydrazide

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Identification
Molecular formula
C13H11N3O2
CAS number
156476-71-8
IUPAC name
N'-(4-nitrosophenyl)benzohydrazide
State
State
N'-(4-nitrosophenyl)benzohydrazide is generally solid at room temperature, manifesting as crystalline powder.
Melting point (Celsius)
218.00
Melting point (Kelvin)
491.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
241.24g/mol
Molar mass
241.2410g/mol
Density
1.2800g/cm3
Appearence

N'-(4-nitrosophenyl)benzohydrazide typically appears as a yellow to orange crystalline powder. The intensity of the color can vary depending on the purity and specific crystallization conditions.

Comment on solubility

Solubility of N'-(4-nitrosophenyl)benzohydrazide

N'-(4-nitrosophenyl)benzohydrazide exhibits specific solubility characteristics that are important for its application in various chemical processes. Understanding its solubility in different solvents can provide insight into its behavior in chemical reactions and formulations.

Solubility Characteristics:

  • Solvent Compatibility: N'-(4-nitrosophenyl)benzohydrazide is generally soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methanol. It has limited solubility in water.
  • Temperature Dependence: The solubility may increase with temperature; heating the solvent can enhance dissolution.
  • pH Sensitivity: The solubility of many nitro compounds can be influenced by the pH of the solution, where a higher pH might promote solubility due to the ionization of functional groups.

In summary, while N'-(4-nitrosophenyl)benzohydrazide is primarily soluble in organic solvents, its interaction with water and the effects of temperature and pH can significantly influence its solubility profile. These factors should be carefully considered when working with this compound in practical applications.

Interesting facts

Interesting Facts About N'-(4-nitrosophenyl)benzohydrazide

N'-(4-nitrosophenyl)benzohydrazide is a fascinating compound, particularly known for its role in organic synthesis and chemical research. Here are some noteworthy aspects of this compound:

  • Versatile Reagent: It serves as a versatile reagent in various chemical reactions. Its ability to participate in nucleophilic addition reactions makes it valuable in synthesizing more complex molecules.
  • Biological Properties: This compound has been explored for its biological activities, particularly its antioxidant and antitumor properties. These potential applications in medicinal chemistry make it a topic of significant interest.
  • Historical Significance: N'-(4-nitrosophenyl)benzohydrazide has historical significance in the study of nitroso compounds, which have been pivotal in understanding chemical reactivity and mechanisms.
  • Colorimetric Applications: Researchers have utilized this compound in colorimetric assays due to its strong chromogenic properties, making it suitable for detecting other chemical species.

In the words of one researcher, “N'-(4-nitrosophenyl)benzohydrazide demonstrates how a simple alteration in structure can yield profound impacts in chemical behavior and application.” This statement encapsulates the essence of organic chemistry—a field where the smallest changes can open the doors to new discoveries.

As a student or scientist, delving into the properties and potential uses of N'-(4-nitrosophenyl)benzohydrazide not only enhances understanding of nitroso compounds but also fosters innovation in chemical research.

Synonyms
Benquinox
495-73-8
Cerenox
Tserenox
Benquinox [ISO]
Benchinox
Benguinox
Cereline
Tillantox
Cereden
Lerenox
CEREDON
Caswell No. 075B
Bayer 15080
Chinonoxime-benzoylhydrazone
Quinone oxime benzoylhydrazone
HSDB 2759
Chinonoxim-benzoylhydrazon
Chinonoxim-benzoylhydrazon [German]
EINECS 207-807-9
p-Benzoquinone oxime benzoylhydrazone
XVO47UK8V8
BAY 15080
EPA Pesticide Chemical Code 281100
1,4-Benzoquinone oxime benzoylhydrazone
BRN 3326107
AI3-25668
1,4-Benzoquinone N'-benzoylhydrazone oxime
BENQUINOX [HSDB]
DTXSID2041624
Benzoic acid, (4-oxo-2,5-cyclohexadien-1-ylidene)hydrazide 4-oxime
0-09-00-00323 (Beilstein Handbook Reference)
Benzoic acid, (4-(hydroxyimino)-2,5-cyclohexadien-1-ylidene) hydrazide
Benzoic acid, (4-(hydroxyimino)-2,5-cyclohexadien-1-ylidene)hydrazide
Benzoic acid, (4-oxo-2,5-cyclohexadien-1-ylidene)hydrazide, oxime
2'-(4-hydroxyiminocyclohexa-2,5-dienylidene)benzohydrazide
BENZOIC ACID (4-(HYDROXYIMINO)-2,5-CYCLOHEXADIEN-1-YLIDENE)HYDRAZIDE
BENZQUINOX
Chinonoximbenzoylhydrazon
Chinonoximebenzoylhydrazone
DTXCID101279988
pBenzoquinone oxime benzoylhydrazone
1,4Benzoquinone oxime benzoylhydrazone
1,4Benzoquinone N'benzoylhydrazone oxime
Benzoic acid, (4oxo2,5cyclohexadien1ylidene)hydrazide 4oxime
Benzoic acid, (4(hydroxyimino)2,5cyclohexadien1ylidene) hydrazide
207-807-9
n'-(4-nitrosophenyl)benzohydrazide
P-BENZOQUINONE 1-BENZOYLHYDRAZON-4-OXIME
COBH
UNII-XVO47UK8V8
SCHEMBL162249
CHEBI:82066
MQIVNMHALJNFMG-UHFFFAOYSA-N
ORLIFVYIUIQGOA-UHFFFAOYSA-N
AAA49573
NS00042553
C18924
Q27155722