Methanamine, N-(2-naphthalenylmethylene)-, N-oxide

Methanamine, N-(2-naphthalenylmethylene)-, N-oxide, with the CAS number 41106-04-1, is a highly specialized and intriguing chemical compound that holds immense potential for researchers and scientists across various fields. This Schiff base derivative, characterized by its unique molecular structure, offers a versatile platform for exploration and innovation.

At the heart of this compound lies a captivating blend of organic chemistry and potential applications. With a molecular formula of C12H11NO and a molecular weight of 185.2218 g/mol, Methanamine, N-(2-naphthalenylmethylene)-, N-oxide presents a distinct combination of a naphthalene moiety, a methanimine group, and an N-oxide functionality. This intricate architecture endows the compound with intriguing chemical properties and reactivity, making it a valuable asset in the realms of pharmaceutical research, organic synthesis, and material science.

The compound's purity, meticulously maintained at 95%, ensures reliable and consistent results in experimental settings. Its InChI code, InChI=1S/C12H11NO/c1-13(14)9-10-6-7-11-4-2-3-5-12(11)8-10/h2-9H,1H3/b13-9+, and its unique MDL number, MFCD09757677, provide researchers with a clear identifier and access to a wealth of technical information to support their investigations.

Pharmaceutical Applications

In the dynamic field of pharmaceutical research, Methanamine, N-(2-naphthalenylmethylene)-, N-oxide holds immense promise. Its distinctive molecular structure and chemical properties make it a valuable building block in the synthesis of novel drug candidates. Researchers can leverage the compound's reactivity and selectivity to develop innovative therapeutics targeting a wide range of health conditions, from neurological disorders to metabolic diseases. The incorporation of the N-oxide moiety, in particular, can contribute to enhanced bioavailability, improved pharmacokinetic profiles, and increased therapeutic efficacy.

The compound's potential extends beyond its use as a synthetic intermediate. Its inherent biological activity may also be explored, as Schiff bases and their N-oxide derivatives have demonstrated intriguing pharmacological properties, such as antimicrobial, anti-inflammatory, and anticancer activities. By delving deeper into the compound's mechanisms of action and structure-activity relationships, researchers can unlock new avenues for therapeutic development.

Organic Synthesis and Material Science

Beyond the pharmaceutical realm, Methanamine, N-(2-naphthalenylmethylene)-, N-oxide finds versatile applications in organic synthesis and material science. Its unique chemical structure and reactivity make it a valuable reagent and building block for the creation of complex organic molecules and advanced materials.

In the field of organic synthesis, researchers can leverage the compound's reactivity to explore a wide range of synthetic transformations, such as condensation reactions, cycloadditions, and nucleophilic additions. The incorporation of the naphthalene and N-oxide moieties can lead to the development of novel heterocyclic compounds, expanding the diversity of molecular scaffolds available for further exploration and application.

In the realm of material science, Methanamine, N-(2-naphthalenylmethylene)-, N-oxide can contribute to the design and synthesis of innovative materials with tailored properties. The compound's aromatic structure and potential for intermolecular interactions may enable the creation of functional polymers, coatings, or advanced composites with enhanced thermal stability, optical characteristics, or mechanical performance.

Safety and Handling

Methanamine, N-(2-naphthalenylmethylene)-, N-oxide is classified as a hazardous compound, with several associated hazard statements, including H302 (Harmful if swallowed), H315 (Causes skin irritation), H319 (Causes serious eye irritation), and H335 (May cause respiratory irritation). Appropriate safety precautions must be taken when handling this compound,