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N-methyl-N-(3-nitrophenyl)nitrous amide

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Identification
Molecular formula
C7H7N3O3
CAS number
6268-68-0
IUPAC name
N-methyl-N-(3-nitrophenyl)nitrous amide
State
State

In its pure form, N-methyl-N-(3-nitrophenyl)nitrous amide is a solid at room temperature. It is typically found as a crystalline compound due to its organic nature and can be stored in this state under appropriate conditions to prevent decomposition or reaction with moisture.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
196.17g/mol
Molar mass
196.1670g/mol
Density
1.2500g/cm3
Appearence

N-methyl-N-(3-nitrophenyl)nitrous amide typically appears as a crystalline solid that can have a slight yellow to tan color due to the presence of the nitro group, which imparts a pale coloration. The compound may not have a strong odor, but safety data should be consulted to ensure safe handling.

Comment on solubility

Solubility of N-methyl-N-(3-nitrophenyl)nitrous amide

N-methyl-N-(3-nitrophenyl)nitrous amide, often referred to in scientific discussions as a nitro-substituted amide, presents some intriguing characteristics in terms of its solubility. This compound exhibits varying levels of solubility in different solvents, which can be attributed to its specific molecular structure and functional groups.

Factors Influencing Solubility:

  • Polarity: The presence of both the nitro group and the amide functional group contributes to its polarity, affecting how well it interacts with solvents.
  • Hydrogen Bonding: The amide group can act as a hydrogen bond donor and acceptor, enhancing solubility in polar solvents.
  • Hydrophobic Interactions: The methyl group and aromatic ring result in hydrophobic character, which may decrease solubility in water but enhance solubility in organic solvents.

As a result, you may find that N-methyl-N-(3-nitrophenyl)nitrous amide is primarily soluble in:

  • Polar organic solvents: Such as ethanol and acetone
  • Aromatic solvents: Such as toluene and dichloromethane

However, its solubility in water is generally limited, which highlights the importance of solvent selection in applications or reactions involving this compound. Understanding these solubility dynamics is crucial for researchers working with this nitro-substituted amide.

Interesting facts

Interesting Facts about N-methyl-N-(3-nitrophenyl)nitrous amide

N-methyl-N-(3-nitrophenyl)nitrous amide is a fascinating compound that is classified as a nitrous amide, showcasing notable chemical properties and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Chemical Structure: The presence of the nitro group (–NO2) on the aromatic ring significantly influences the compound's reactivity and interactions. The nitro group is known for its electron-withdrawing effects, which can stabilize certain reaction intermediates.
  • Applications in Research: This compound has been a subject of interest in synthetic organic chemistry. Its unique structure provides useful pathways for developing new materials or pharmaceuticals, offering a template for further modifications in drug design.
  • Potential Biological Activity: Compounds like N-methyl-N-(3-nitrophenyl)nitrous amide are often explored for biological activities. Researchers investigate compounds with nitro groups for their potential to exhibit antimicrobial, anti-inflammatory, or anticancer properties, making this class of compounds crucial in medicinal chemistry.
  • Safety Considerations: As with many nitro compounds, safety precautions are essential in handling N-methyl-N-(3-nitrophenyl)nitrous amide. Its potential reactivity and the effects of nitro groups on stability must be carefully managed during synthesis and application.
  • Chemical Reactions: This compound can undergo various reactions typical of amides and nitro compounds, such as nucleophilic substitution or reduction processes. These reactions can be pivotal in synthesizing further derivatives or in studying reaction mechanisms.

In conclusion, N-methyl-N-(3-nitrophenyl)nitrous amide illustrates the intricate world of organic chemistry, where structure informs function. As researchers continue to uncover its properties and potential applications, it stands as a testament to the ongoing exploration within the field.

Synonyms
ANILINE, N-METHYL-m-NITRO-N-NITROSO-
BRN 1842298
N-Methyl-m-nitro-N-nitrosoaniline
18600-50-5
DTXSID10171831
4-16-00-00869 (Beilstein Handbook Reference)
DTXCID4094322