2-Morpholinoimino-1-(4-nitrophenyl)ethanone

Identification

Molecular formula

C₁₂H₁₃N₃O₄

CAS number

67660-80-2

IUPAC name

2-morpholinoimino-1-(4-nitrophenyl)ethanone

State

At room temperature, this compound is typically a crystalline solid.

Melting point (Celsius)

137.00

Melting point (Kelvin)

410.15

Boiling point (Celsius)

262.00

Boiling point (Kelvin)

535.15

General information

Molecular weight

277.28g/mol

Molar mass

277.2760g/mol

Density

1.4000g/cm³

Appearence

The compound generally appears as a crystalline solid. The color may vary from off-white to yellow, reflecting the presence of the nitro group in the structure.

Comment on solubility

Solubility of 2-morpholinoimino-1-(4-nitrophenyl)ethanone

When considering the solubility of 2-morpholinoimino-1-(4-nitrophenyl)ethanone, several factors come into play. This compound is known for its organic nature, which can influence its interaction with various solvents.

Key Solubility Insights:

Polar and Non-polar Solvents: It is generally expected that 2-morpholinoimino-1-(4-nitrophenyl)ethanone will exhibit varying degrees of solubility in different solvent types. Typically, such compounds are more soluble in polar solvents like alcohols or dimethyl sulfoxide (DMSO).
Hydrogen Bonding: The presence of a morpholine moiety allows for potential hydrogen bonding, enhancing solubility in polar environments.
Electrostatic Interactions: With the nitrophenyl group, electrostatic interactions may facilitate solubility, particularly in solvent systems that can stabilize such polar groups.

Overall, while the specific solubility parameters of 2-morpholinoimino-1-(4-nitrophenyl)ethanone may not be extensively documented, it is reasonable to anticipate enhanced solubility in polar solvents due to its structural functionalities. As a rule of thumb in chemistry, “like dissolves like,” which suggests choosing solvents with similar polarities to that of the compound will yield the best results in solubility.

Interesting facts

Interesting Facts about 2-Morpholinoimino-1-(4-nitrophenyl)ethanone

2-Morpholinoimino-1-(4-nitrophenyl)ethanone is a fascinating compound that bridges the domains of organic chemistry and medicinal applications. Its unique structure allows it to interact with biological systems, making it a subject of interest in pharmacology and materials science.

Key Highlights:

Pharmacological Significance: This compound is often investigated for its potential pharmacological properties, particularly its role as an intermediate in the synthesis of bioactive molecules.
Versatile Applications: Due to its morpholino group, it may exhibit enhanced stability and solubility, thus increasing its efficacy in drug formulations.
Electrophilic Nature: The presence of the nitrophenyl group significantly influences the reactivity of the compound, making it a key player in electrophilic substitution reactions.
Research Potential: Scientists are exploring its use in developing new therapeutic agents, particularly in targeting specific enzymes associated with various diseases.
Reaction Pathways: The compound can serve as a precursor in numerous synthetic pathways, facilitating the creation of complex organic structures.

In conclusion, 2-Morpholinoimino-1-(4-nitrophenyl)ethanone exemplifies the intricate relationship between structure and function in chemical compounds. As noted by researchers, "The design of small molecules can lead to significant advancements in treating complex biological conditions." The exploration of its properties and potential applications continues to be a vibrant area of study for chemists and pharmaceutical scientists alike.