N-Methyl-4-nitrophthalimide CAS:1515-72-6
Catalog Number | XD95704 |
Product Name | N-Methyl-4-nitrophthalimide |
CAS | 1515-72-6 |
Molecular Formula | C12H13NO2 |
Molecular Weight | 203.24 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
N-Methyl-4-nitrophthalimide is a chemical compound that consists of a phthalimide ring with a methyl group (-CH3) and a nitro group (-NO2) attached to it. It possesses several notable effects and applications:Reactivity in organic synthesis: N-Methyl-4-nitrophthalimide is often used as a reagent in organic synthesis reactions. The nitro group present in the compound makes it a strong oxidizing agent, capable of undergoing various reactions such as reduction and nucleophilic substitution. It can be used to introduce the N-methyl-4-nitrophthalimide moiety into target molecules, creating new compounds with desirable properties.Biological activity: N-Methyl-4-nitrophthalimide and its derivatives have been studied for their potential biological activities. Researchers have found that certain derivatives of the compound exhibit interesting antimicrobial, antiviral, antiproliferative, and anticancer properties. These findings suggest that N-Methyl-4-nitrophthalimide compounds may have potential applications in drug discovery and development.Impact on hydrogen bonding: The N-Methyl-4-nitrophthalimide moiety is known to participate in intermolecular hydrogen bonding interactions. This property is important in determining the physical and chemical characteristics of compounds containing this group. Hydrogen bonding can influence factors such as solubility, melting point, stability, and crystal structure.Use as a targeted anticancer agent: Some studies have explored the use of N-Methyl-4-nitrophthalimide derivatives as targeted anticancer agents. By attaching specific ligands to the phthalimide core, researchers can create compounds that selectively target cancer cells, leading to increased efficacy and reduced side effects compared to traditional chemotherapy drugs. This approach takes advantage of the fact that many cancer cells overexpress certain receptors or antigens that can be targeted by ligands.Safety considerations: As with any chemical compound, precautions should be taken when handling N-Methyl-4-nitrophthalimide. It is important to follow proper safety measures, such as wearing appropriate personal protective equipment and working in a well-ventilated area. Additionally, the potential toxicity and environmental impact of this compound should be considered, and proper disposal methods should be followed to minimize any adverse effects.In summary, N-Methyl-4-nitrophthalimide exhibits reactivity in organic synthesis, shows potential biological activities, affects hydrogen bonding interactions, and may have applications as a targeted anticancer agent. It is important to handle this compound with caution and adhere to safety measures. Further research on its biological properties and potential applications is ongoing.