Interesting facts
Interesting Facts about 1-(5-Nitro-2-furyl)-N-phenyl-methanimine
1-(5-Nitro-2-furyl)-N-phenyl-methanimine, often referred to as a nitro-containing furan derivative, is a compound of significant interest in both organic chemistry and medicinal research. Here are some intriguing aspects of this compound:
- Potential Pharmaceutical Applications: Due to the presence of the nitro group and the furan ring, this compound exhibits a variety of biological activities that make it a candidate for pharmaceutical research. Compounds with similar structures have been studied for their potential as anti-cancer agents.
- Importance of Furan Rings: Furans are a class of organic compounds known for their stability and reactivity. The furan ring in this compound contributes to its unique chemical properties and opens avenues for further chemical transformations.
- Synthetic Versatility: The synthesis of 1-(5-nitro-2-furyl)-N-phenyl-methanimine can be achieved through various methods, showcasing the versatility of reaction conditions and substrates in organic synthesis.
- Electrophilic Character: The presence of the nitro group on the furan ring enhances the electrophilic character of certain areas in the molecule, which may facilitate interactions with nucleophiles in biological systems, potentially influencing pharmacodynamics.
- Research Opportunities: The compound’s unique structure provides an exciting platform for research into new derivatives that may enhance desired biological activities or minimize side effects. Scientists often explore structure-activity relationships to optimize such compounds.
As a scientist or a chemistry student, the study of 1-(5-nitro-2-furyl)-N-phenyl-methanimine presents a fascinating intersection of organic synthesis, medicinal chemistry, and the exploration of new therapeutic agents. It exemplifies how subtle modifications in molecular structure can lead to substantial changes in reactivity and biological activity.
Synonyms
N-(5-Nitrofurfurylidene)aniline
156-44-5
BRN 0174736
ANILINE, N-(5-NITROFURFURYLIDENE)-
N-((5-Nitro-2-furanyl)methylene)benzenamine
Benzenamine, N-((5-nitro-2-furanyl)methylene)-
DTXSID701303561
5-17-09-00325 (Beilstein Handbook Reference)
N-((5-Nitrofuran-2-yl)methylene)aniline
DTXCID601733593
STK756698
AKOS001733642
EU-0051645
N-[(E)-(5-nitro-2-furyl)methylidene]aniline
N-[(E)-(5-nitrofuran-2-yl)methylidene]aniline
(E)-1-(5-NITROFURAN-2-YL)-N-PHENYLMETHANIMINE
Benzenamine, N-((5-nitro-2-furanyl)methylene)-(9CI)
660-250-7
Solubility of 1-(5-nitro-2-furyl)-N-phenyl-methanimine
The solubility of 1-(5-nitro-2-furyl)-N-phenyl-methanimine can be affected by various factors, including its molecular structure and interactions with solvents. Here are some key points to consider:
Ultimately, while specific numerical solubility data for 1-(5-nitro-2-furyl)-N-phenyl-methanimine may not be readily available, understanding the underlying principles of solubility can offer insights into its behavior in different solvent systems. As stated, “Like dissolves like” is a fundamental rule in chemistry that underpins solubility trends across various compounds.