Interesting facts
Interesting Facts about N-(4-fluorophenyl)-N-methyl-nitrous amide
N-(4-fluorophenyl)-N-methyl-nitrous amide is a fascinating compound that finds its relevance in various fields of chemistry and industry. Here are some compelling details that showcase its significance and unique characteristics:
- Origin: This compound represents a class of nitrous amides, which are notable for their role in organic synthesis. They are essential in designing and preparing other biologically active molecules through functional group transformations.
- Fluorine's Role: The presence of the 4-fluorophenyl group is particularly interesting as fluorine is known to alter the properties of organic compounds significantly. This can lead to enhanced biological activity or modifications in reactivity, making it a popular choice in medicinal chemistry.
- Applications: N-(4-fluorophenyl)-N-methyl-nitrous amide serves pivotal functions in the development of pharmaceuticals. Its derivatives may be researched for their potential use in treatments, especially in areas targeting metabolic diseases.
- Synthetic Utility: As a nitrous amide, this compound can be employed in various synthetic pathways. Its versatility allows chemists to create a wide array of conjugated systems, which are crucial in the advancement of complex molecules.
- Stability and Safety: Understanding the stability of nitrous amides, including N-(4-fluorophenyl)-N-methyl-nitrous amide, is vital for ensuring safe handling in laboratories. Its kinetic properties can affect how it behaves under different conditions.
- Research Potential: Ongoing research exploring the structure-activity relationship (SAR) of compounds similar to N-(4-fluorophenyl)-N-methyl-nitrous amide could lead to significant breakthroughs in drug design and development.
In summary, N-(4-fluorophenyl)-N-methyl-nitrous amide is more than just a chemical formula; it opens up a realm of possibilities in organic synthesis and pharmaceuticals. The study of such compounds not only enhances our understanding of chemical interactions but also propels innovation in medical therapies.
Synonyms
N-Nitroso-N-methyl-4-fluoroaniline
937-25-7
p-Fluoro-N-methyl-N-nitrosoaniline
N-(4-fluorophenyl)-N-methylnitrous amide
BRN 1841690
ANILINE, p-FLUORO-N-METHYL-N-NITROSO-
DTXSID9021001
4-Fluoro-N-methyl-N-nitrosobenzenamine
p-FNMA
DTXCID501001
881-074-9
4-fluoro-N-methyl-N-nitrosoaniline
9LSX9S4XBW
UNII-9LSX9S4XBW
Methyl(4-fluorophenyl)nitrosamine
AKOS006272804
Nitroso-N-methyl-4-fluoroaniline, N-
Benzenamine, 4-fluoro-N-methyl-N-nitroso-
F81208
EN300-7691313
Solubility of N-(4-fluorophenyl)-N-methyl-nitrous amide
N-(4-fluorophenyl)-N-methyl-nitrous amide, with the chemical formula C8H9F1N2O, exhibits interesting solubility characteristics that are influenced by its structural components.
In general, the solubility of this compound can be summarized as follows:
To conclude, as with many organic compounds, the solubility of N-(4-fluorophenyl)-N-methyl-nitrous amide is primarily dictated by its structural features and the solvent's properties. Its polar nature fosters solubility in polar media while limiting its dissolvability in non-polar environments. This dual behavior is a key aspect to consider in practical applications and further research.