Cas no 1432-45-7 (2-Propenamide,N-acetyl-)

2-Propenamide, N-acetyl-, also known as N-acryloylamide, is a versatile acrylamide derivative with applications in polymer chemistry and material science. Its key advantages include high reactivity due to the presence of both acrylamide and acetyl functional groups, enabling efficient copolymerization with other monomers. This compound is particularly useful in the synthesis of hydrogels, adhesives, and coatings, where its ability to form cross-linked networks enhances mechanical strength and stability. Its compatibility with aqueous systems and controlled polymerization conditions makes it suitable for biomedical and industrial applications. The acetyl group provides additional chemical functionality, allowing for further modification to tailor material properties.
2-Propenamide,N-acetyl- structure
2-Propenamide,N-acetyl- structure
Product Name:2-Propenamide,N-acetyl-
CAS No:1432-45-7
MF:C5H7NO2
MW:113.114581346512
CID:222358
PubChem ID:307934
Update Time:2025-10-25

2-Propenamide,N-acetyl- Chemical and Physical Properties

Names and Identifiers

    • 2-Propenamide,N-acetyl-
    • N-acetylprop-2-enamide
    • AC1L7BTS
    • acetacrylimide
    • Acetamidoacrylsaeure
    • Acetyl-acryloyl-amin
    • acetyl-acryloyl-amine
    • N-Acetyl-acrylamid
    • N-acetylacrylamide
    • NSC206297
    • N-(PROP-2-ENOYL)ACETAMIDE
    • NSC-206297
    • SCHEMBL372428
    • EN300-5085858
    • NSC 206297
    • DTXSID10308660
    • 1432-45-7
    • Inchi: 1S/C5H7NO2/c1-3-5(8)6-4(2)7/h3H,1H2,2H3,(H,6,7,8)
    • InChI Key: RUSRUYULUAYXIP-UHFFFAOYSA-N
    • SMILES: O=C(C)NC(C=C)=O

Computed Properties

  • Exact Mass: 113.04771
  • Monoisotopic Mass: 113.048
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 1
  • Complexity: 128
  • 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: -0.1
  • Topological Polar Surface Area: 46.2?2

Experimental Properties

  • Density: 1.035
  • Boiling Point: 226°C at 760 mmHg
  • Flash Point: 112.1°C
  • Refractive Index: 1.436
  • PSA: 46.17
  • LogP: 0.22600

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Additional information on 2-Propenamide,N-acetyl-

Professional Introduction to 2-Propenamide, N-acetyl- (CAS No. 1432-45-7)

2-Propenamide, N-acetyl-, identified by its Chemical Abstracts Service (CAS) number 1432-45-7, is a compound of significant interest in the field of organic chemistry and pharmaceutical research. This amide derivative, characterized by its acetylated propenamide structure, has garnered attention due to its versatile applications and potential in synthetic chemistry and drug development. The compound’s unique molecular architecture, featuring both a propenyl group and an acetyl moiety, makes it a valuable intermediate in the synthesis of more complex molecules.

The structural properties of 2-Propenamide, N-acetyl- contribute to its reactivity and utility in various chemical transformations. The presence of the amide bond not only facilitates nucleophilic acyl substitution reactions but also allows for further functionalization through hydrolysis or reduction. These characteristics make it a promising candidate for use in the synthesis of peptidomimetics and other bioactive molecules. Recent advancements in medicinal chemistry have highlighted the importance of such intermediates in the development of novel therapeutic agents.

In the realm of pharmaceutical research, 2-Propenamide, N-acetyl- has been explored as a precursor in the synthesis of bioactive peptides and small-molecule drugs. Its ability to serve as a scaffold for structural modifications allows chemists to tailor properties such as solubility, bioavailability, and metabolic stability. For instance, studies have demonstrated its role in the development of protease inhibitors, where the acetylated propenamide core contributes to enhanced binding affinity and selectivity. The compound’s versatility is further underscored by its application in peptidomimetic chemistry, where it aids in creating molecules that mimic the biological activity of natural peptides while avoiding their drawbacks.

The chemical behavior of 2-Propenamide, N-acetyl- is also influenced by its interaction with biological systems. Research has indicated that this compound can exhibit inhibitory effects on certain enzymatic pathways, making it a potential lead compound for drug discovery programs targeting inflammatory diseases or infectious agents. The acetyl group, in particular, plays a crucial role in modulating these interactions by influencing both electronic and steric properties. This has led to investigations into its derivatives as candidates for antimicrobial or anti-inflammatory therapies.

From a synthetic chemistry perspective, 2-Propenamide, N-acetyl- serves as a key building block for more complex structures. Its reactivity allows for the introduction of additional functional groups through various coupling reactions, such as amide bond formation or alkylation processes. These synthetic pathways are essential in constructing molecules with tailored pharmacological profiles. The compound’s stability under standard reaction conditions further enhances its appeal as an intermediate in large-scale organic synthesis.

The industrial relevance of 2-Propenamide, N-acetyl- is also reflected in its use as a starting material for specialty chemicals. Its incorporation into more sophisticated derivatives has led to the development of materials with applications ranging from agrochemicals to advanced polymers. The ability to modify its structure while retaining core functionalities makes it indispensable in industrial processes where precision and efficiency are paramount.

Recent studies have further expanded the understanding of 2-Propenamide, N-acetyl-‘s role in medicinal chemistry. Researchers have leveraged computational methods to predict its interactions with biological targets, providing insights into potential drug-like properties. These computational approaches have complemented experimental efforts, enabling faster screening of derivatives with improved efficacy and reduced toxicity. The integration of machine learning models with traditional chemical intuition has accelerated the discovery pipeline for new therapeutic agents derived from this compound.

The environmental impact of utilizing 2-Propenamide, N-acetyl- as a chemical intermediate has also been examined. Efforts to develop greener synthetic routes have focused on optimizing reaction conditions to minimize waste and energy consumption. Such initiatives align with broader trends in sustainable chemistry, where minimizing environmental footprints is a priority without compromising yield or purity. Advances in catalytic systems have been particularly instrumental in achieving these goals.

Future directions for research involving 2-Propenamide, N-acetyl- include exploring its potential applications in nanotechnology and material science. The compound’s ability to form stable complexes with other molecules makes it suitable for use as a cross-linking agent or functional additive in advanced materials. Additionally, its role as a precursor for bioconjugates has implications for diagnostic imaging and targeted drug delivery systems.

In conclusion,2-Propenamide,N-acetyl-(CAS No 1432 45 7) remains a pivotal compound across multiple domains of chemistry and pharmacology Its unique structural features offer unparalleled flexibility in synthetic applications while its biological relevance positions it as a cornerstone for innovative drug discovery Efforts continue to optimize its production methods enhance understanding through interdisciplinary research ensuring that this versatile molecule continues to contribute significantly to scientific progress

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