Cas no 98278-03-6 (n-ethyl-n-methylpropanamide)

N-Ethyl-N-methylpropanamide is a tertiary amide characterized by its clear liquid form and moderate polarity. Its structure, featuring an ethyl and methyl group attached to the nitrogen atom, enhances solubility in both polar and nonpolar solvents, making it a versatile intermediate in organic synthesis. The compound exhibits stability under standard conditions and is often employed in pharmaceutical and agrochemical applications due to its reactivity as an acylating agent. Its low volatility and compatibility with a range of reagents contribute to its utility in controlled reactions. The absence of reactive side groups minimizes unwanted byproducts, ensuring efficient process yields.
n-ethyl-n-methylpropanamide structure
n-ethyl-n-methylpropanamide structure
Product Name:n-ethyl-n-methylpropanamide
CAS No:98278-03-6
MF:C6H13NO
MW:115.173521757126
CID:860668
PubChem ID:18387020
Update Time:2025-05-24

n-ethyl-n-methylpropanamide Chemical and Physical Properties

Names and Identifiers

    • n-ethyl-n-methylpropanamide
    • SCHEMBL792423
    • BS-48253
    • N-methyl-N-ethyl-propanamide
    • F74635
    • N-Ethyl-N-methylpropionamide
    • AKOS009207636
    • 98278-03-6
    • Inchi: 1S/C6H13NO/c1-4-6(8)7(3)5-2/h4-5H2,1-3H3
    • InChI Key: GHVUKOCVBVUUGS-UHFFFAOYSA-N
    • SMILES: O=C(CC)N(C)CC

Computed Properties

  • Exact Mass: 115.1
  • Monoisotopic Mass: 115.1
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 2
  • Complexity: 80.6
  • 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
  • Topological Polar Surface Area: 20.3A^2
  • XLogP3: 0.6

Experimental Properties

  • Density: 0.873
  • Boiling Point: 181.928°C at 760 mmHg
  • Flash Point: 69.316°C
  • Refractive Index: 1.423

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Additional information on n-ethyl-n-methylpropanamide

N-Ethyl-N-Methylpropanamide: A Comprehensive Overview

N-Ethyl-N-Methylpropanamide, also known by its CAS No. 98278-03-6, is a versatile organic compound with significant applications in various industries. This compound, which belongs to the family of amides, has gained attention due to its unique chemical properties and potential uses in pharmaceuticals, agriculture, and materials science. In recent years, advancements in synthetic chemistry and material engineering have further expanded its utility, making it a subject of interest for researchers and industry professionals alike.

The molecular structure of n-ethyl-n-methylpropanamide consists of a propanamide backbone with ethyl and methyl substituents on the nitrogen atom. This structure contributes to its stability and reactivity, making it suitable for various chemical transformations. Recent studies have explored its role as a precursor in the synthesis of bioactive compounds, where its ability to participate in nucleophilic substitutions and condensation reactions has been particularly valuable. For instance, researchers have utilized it in the development of novel agrochemicals that exhibit improved efficacy against plant pathogens.

One of the most promising areas of research involving n-ethyl-n-methylpropanamide is its application in drug delivery systems. Scientists have investigated its potential as a carrier molecule due to its ability to enhance the solubility and bioavailability of hydrophobic drugs. A study published in 2023 demonstrated that incorporating this compound into lipid-based nanoparticles significantly improved the delivery efficiency of antitumor agents, paving the way for more effective cancer treatments.

In addition to its pharmaceutical applications, n-ethyl-n-methylpropanamide has found utility in the field of polymer chemistry. Researchers have explored its use as a building block for synthesizing biodegradable polymers, which are increasingly sought after in sustainable materials development. These polymers exhibit excellent mechanical properties and biocompatibility, making them ideal candidates for biomedical applications such as tissue engineering scaffolds and drug delivery devices.

The environmental impact of n-ethyl-n-methylpropanamide has also been a topic of interest. Studies have shown that it is biodegradable under certain conditions, which aligns with the growing demand for eco-friendly chemical compounds. However, further research is needed to optimize its degradation pathways and minimize any potential ecological risks.

From an industrial perspective, the synthesis of n-ethyl-n-methylpropanamide has been streamlined through advancements in catalytic processes. Modern methods employ efficient catalysts that reduce reaction times and energy consumption, making large-scale production more feasible and cost-effective. This has contributed to its widespread availability in global markets, catering to diverse industrial needs.

In conclusion, n-ethyl-n-methylpropanamide, with its CAS No. 98278-03-6, stands as a testament to the ongoing innovation in chemical science. Its multifaceted applications across pharmaceuticals, materials science, and agriculture underscore its importance as a key compound in modern chemistry. As research continues to uncover new potentials for this compound, it is poised to play an even greater role in shaping future technologies and industries.

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