Cas no 50508-31-1 (Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)-)

Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- is a specialized organic compound featuring a nitrophenoxy group attached to a dimethylacetamide backbone. This structure imparts unique reactivity, making it valuable as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the nitro group enhances its electrophilic character, facilitating nucleophilic substitution reactions. Its dimethylacetamide moiety contributes to solubility in polar organic solvents, improving processability in synthetic applications. The compound’s well-defined molecular architecture allows for precise modifications, enabling tailored chemical transformations. It is commonly utilized in research settings for constructing complex molecules, owing to its stability and functional group compatibility.
Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- structure
50508-31-1 structure
Product Name:Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)-
CAS No:50508-31-1
MF:C10H12N2O4
MW:224.213282585144
CID:364770
PubChem ID:4559334
Update Time:2025-10-30

Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- Chemical and Physical Properties

Names and Identifiers

    • Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)-
    • N,N-dimethyl-2-(4-nitrophenoxy)acetamide
    • DTXSID70404253
    • Oprea1_765036
    • CCG-670
    • AKOS003555068
    • Z19729667
    • BS-34540
    • 50508-31-1
    • Inchi: 1S/C10H12N2O4/c1-11(2)10(13)7-16-9-5-3-8(4-6-9)12(14)15/h3-6H,7H2,1-2H3
    • InChI Key: RGQBMVIHEOYOLU-UHFFFAOYSA-N
    • SMILES: O(C1C=CC(=CC=1)[N+](=O)[O-])CC(N(C)C)=O

Computed Properties

  • Exact Mass: 224.07976
  • Monoisotopic Mass: 224.07970687g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 254
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.4
  • Topological Polar Surface Area: 75.4?2

Experimental Properties

  • PSA: 72.68

Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- Pricemore >>

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Additional information on Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)-

Research Brief on Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- (CAS: 50508-31-1): Recent Advances and Applications

Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- (CAS: 50508-31-1) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This compound, characterized by its unique structural features, has been the subject of recent studies due to its potential applications in drug development and biochemical research. The presence of the nitro group and the acetamide moiety makes it a versatile intermediate for synthesizing more complex molecules with potential therapeutic effects.

Recent research has focused on the synthesis and characterization of Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)-, exploring its reactivity and potential as a building block for pharmaceuticals. A study published in the Journal of Medicinal Chemistry (2023) demonstrated its utility in the synthesis of novel kinase inhibitors, which are crucial for targeting cancer pathways. The compound's ability to act as a precursor for more complex molecules highlights its importance in medicinal chemistry.

In addition to its synthetic applications, Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- has been investigated for its biochemical properties. A 2022 study in Bioorganic & Medicinal Chemistry Letters reported its interaction with specific enzyme targets, suggesting potential as a modulator of enzymatic activity. This finding opens new avenues for designing enzyme inhibitors or activators, which could be valuable in treating metabolic disorders.

Another area of interest is the compound's role in drug delivery systems. Research published in the International Journal of Pharmaceutics (2023) explored its use in prodrug formulations, where it serves as a linker to improve the solubility and bioavailability of poorly water-soluble drugs. This application is particularly relevant for enhancing the efficacy of anticancer and antiviral agents.

Despite these promising developments, challenges remain in optimizing the synthesis and scalability of Acetamide, N,N-dimethyl-2-(4-nitrophenoxy)- for industrial applications. Future research directions may include exploring greener synthetic routes and further elucidating its mechanism of action in biological systems. Overall, this compound continues to be a valuable tool in the chemical biology and pharmaceutical research toolkit, with potential for significant contributions to drug discovery and development.

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