Cas no 16151-14-7 (3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one)

3-Acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one is a heterocyclic compound featuring a dihydropyridinone core with acetyl and methyl substituents. This structure imparts unique reactivity, making it a valuable intermediate in organic synthesis, particularly for the preparation of pharmaceuticals and agrochemicals. The acetyl group enhances electrophilic character, facilitating further functionalization, while the methyl groups contribute to steric and electronic modulation. Its stable dihydropyridinone scaffold is advantageous for constructing complex nitrogen-containing frameworks. The compound’s well-defined crystalline form ensures consistent purity, critical for precise synthetic applications. Suitable for use in medicinal chemistry and material science, it offers a balance of reactivity and stability for targeted molecular transformations.
3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one structure
16151-14-7 structure
Product Name:3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one
CAS No:16151-14-7
MF:C9H11NO2
MW:165.189142465591
MDL:MFCD00775755
CID:904596
PubChem ID:2302267
Update Time:2025-10-29

3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one Chemical and Physical Properties

Names and Identifiers

    • IFLAB-BB F2113-0039
    • 3-Acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one
    • 2-Hydroxy-3-acetyl-4,6-dimethylpyridin
    • 3-acetyl-2,4-dimethyl-2-(1H)pyridone
    • 3-acetyl-4,6-dimethyl-2(1H)-pyridinone
    • 3-acetyl-4,6-dimethyl-2(1H)-pyridone
    • 3-acetyl-4,6-dimethyl-2-pyridone
    • 3-acetyl-4,6-dimethylpyridin-2(1H)-one
    • AC1M4779
    • CTK0E6490
    • F2113-0039
    • STK373038
    • SureCN4519599
    • 3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one
    • MDL: MFCD00775755
    • Inchi: 1S/C9H11NO2/c1-5-4-6(2)10-9(12)8(5)7(3)11/h4H,1-3H3,(H,10,12)
    • InChI Key: FPZYYMHZCULYSO-UHFFFAOYSA-N
    • SMILES: O=C1C(C(C)=O)=C(C)C=C(C)N1

Computed Properties

  • Exact Mass: 165.07903
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1

Experimental Properties

  • PSA: 46.17

3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one Pricemore >>

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Additional information on 3-acetyl-4,6-dimethyl-1,2-dihydropyridin-2-one

Comprehensive Overview of IFLAB-BB F2113-0039 (CAS No. 16151-14-7): Properties, Applications, and Market Insights

IFLAB-BB F2113-0039 (CAS No. 16151-14-7) is a specialized chemical compound widely recognized for its unique properties and versatile applications across multiple industries. With increasing interest in high-performance materials and sustainable chemistry, this compound has garnered attention from researchers and manufacturers alike. Its molecular structure and functional characteristics make it a valuable component in formulations requiring precision and reliability.

The chemical industry is currently focusing on eco-friendly alternatives and energy-efficient processes, and IFLAB-BB F2113-0039 aligns well with these trends. Its stability under various conditions and compatibility with other materials make it a preferred choice for applications in advanced coatings, adhesives, and specialty polymers. Researchers are also exploring its potential in biomedical applications, where its non-toxic profile and performance under physiological conditions are highly advantageous.

One of the key advantages of IFLAB-BB F2113-0039 is its adaptability in nanotechnology and material science. As industries seek to develop lighter, stronger, and more durable materials, this compound offers a promising solution. Its role in enhancing the properties of composite materials has been particularly noteworthy, with studies highlighting improvements in tensile strength, thermal resistance, and chemical inertness.

In the context of green chemistry, IFLAB-BB F2113-0039 stands out due to its low environmental impact and biodegradability. Manufacturers are increasingly adopting this compound to meet stringent regulatory standards and consumer demand for sustainable products. Its use in water-based formulations further underscores its compatibility with environmentally conscious production methods.

Market trends indicate a growing demand for IFLAB-BB F2113-0039 in the electronics industry, where it is utilized in the production of flexible circuits and conductive inks. The rise of wearable technology and IoT devices has further amplified its relevance, as these applications require materials that combine flexibility with high performance. Additionally, its role in 3D printing materials is being explored, offering new possibilities for customized manufacturing.

From a research perspective, IFLAB-BB F2113-0039 is the subject of ongoing studies aimed at unlocking its full potential. Scientists are investigating its interactions with other compounds to develop next-generation materials with enhanced functionalities. The compound's ability to form stable complexes and its reactivity under controlled conditions make it a valuable tool in chemical synthesis and catalysis.

Quality control and standardization are critical when working with IFLAB-BB F2113-0039, as its performance is highly dependent on purity and formulation. Reputable suppliers provide detailed technical data sheets and certificates of analysis to ensure consistency and reliability. This level of transparency is essential for industries where precision and reproducibility are paramount.

In summary, IFLAB-BB F2113-0039 (CAS No. 16151-14-7) represents a cutting-edge solution for modern chemical challenges. Its diverse applications, from industrial manufacturing to emerging technologies, highlight its versatility and importance. As the demand for innovative and sustainable materials grows, this compound is poised to play a pivotal role in shaping the future of multiple industries.

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