Cas no 36660-46-5 (2-(naphthalen-2-yl)acetamide)

2-(Naphthalen-2-yl)acetamide is a naphthalene-derived organic compound featuring an acetamide functional group at the 2-position of the naphthalene ring. This structure imparts versatility in synthetic applications, particularly as an intermediate in pharmaceuticals, agrochemicals, and material science. Its aromatic backbone enhances stability, while the acetamide group offers reactivity for further functionalization, such as condensation or substitution reactions. The compound’s well-defined crystalline properties facilitate purification and characterization, ensuring consistency in research and industrial processes. Its compatibility with diverse reaction conditions makes it valuable for developing biologically active molecules or advanced materials. Suitable for controlled-scale synthesis, it is often utilized in exploratory chemistry and target-oriented synthesis.
2-(naphthalen-2-yl)acetamide structure
2-(naphthalen-2-yl)acetamide structure
Product Name:2-(naphthalen-2-yl)acetamide
CAS No:36660-46-5
MF:C12H11NO
MW:185.221843004227
MDL:MFCD11643177
CID:921529
PubChem ID:95293
Update Time:2025-05-28

2-(naphthalen-2-yl)acetamide Chemical and Physical Properties

Names and Identifiers

    • 2-naphthalen-2-ylacetamide
    • 2-Naphthaleneacetamide
    • [2]naphthyl-acetic acid amide
    • [2]Naphthyl-essigsaeure-amid
    • 2-(naphthalen-2-yl)acetamide
    • 2-(naphthalene-2-yl) acetamide
    • 2-(naphthalene-2-yl)-acetamide
    • 2-naphthylacetamide
    • AC1L3TZI
    • AC1Q4ZL2
    • AC1Q5J7W
    • CTK1C2532
    • NSC28055
    • SureCN1533677
    • CS-0258010
    • naphthalene-2-acetamide
    • I(2)-Acetylaminonaphthalin
    • G25869
    • 2-Naphthalen-2-yl-acetamide
    • Z33546100
    • NSC-28055
    • 2-(2-naphthyl)acetamide
    • EN300-68829
    • SCHEMBL1533677
    • AKOS008937866
    • .BETA.-NAPHTHYLACETAMIDE
    • DA-06399
    • UNII-1Q5KZ5BQH2
    • 36660-46-5
    • 1Q5KZ5BQH2
    • MFCD11643177
    • LVYUDSCQJGQXBI-UHFFFAOYSA-N
    • NSC 28055
    • DTXSID40190116
    • MDL: MFCD11643177
    • Inchi: 1S/C12H11NO/c13-12(14)8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2,(H2,13,14)
    • InChI Key: LVYUDSCQJGQXBI-UHFFFAOYSA-N
    • SMILES: O=C(CC1C=CC2C=CC=CC=2C=1)N

Computed Properties

  • Exact Mass: 185.08413
  • Monoisotopic Mass: 185.084063974g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 214
  • 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: 2.2
  • Topological Polar Surface Area: 43.1?2

Experimental Properties

  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 420.6±24.0 °C at 760 mmHg
  • Flash Point: 208.2±22.9 °C
  • PSA: 43.09
  • LogP: 2.56790
  • Vapor Pressure: 0.0±1.0 mmHg at 25°C

2-(naphthalen-2-yl)acetamide Security Information

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2-(naphthalen-2-yl)acetamide Suppliers

Amadis Chemical Company Limited
Gold Member
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(CAS:36660-46-5)2-(naphthalen-2-yl)acetamide
Order Number:A1159362
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 23:53
Price ($):276.0

Additional information on 2-(naphthalen-2-yl)acetamide

Comprehensive Guide to 2-(Naphthalen-2-yl)acetamide (CAS No. 36660-46-5): Properties, Applications, and Research Insights

2-(Naphthalen-2-yl)acetamide (CAS No. 36660-46-5) is a specialized organic compound gaining attention in pharmaceutical and material science research. This naphthalene derivative, characterized by its acetamide functional group, serves as a versatile intermediate in synthetic chemistry. With the rising demand for naphthalene-based compounds in drug discovery, this molecule has become a subject of interest for researchers exploring structure-activity relationships and bioactive molecule design.

The compound's molecular structure combines a naphthalene ring system with an acetamide moiety, offering unique electronic and steric properties. Recent studies highlight its potential as a building block for fluorescent probes and small-molecule sensors, aligning with current trends in chemical biology and diagnostic imaging. Researchers are particularly interested in its photophysical characteristics, which may contribute to advancements in organic electronics and optoelectronic materials.

In pharmaceutical applications, 2-(naphthalen-2-yl)acetamide derivatives are being investigated for their biological activity profiles. The compound's structural features make it a valuable scaffold for developing enzyme inhibitors and receptor modulators. Current literature suggests potential applications in neurological research, with particular focus on its molecular interactions with biological targets. These developments correspond with growing public interest in neurodegenerative disease research and central nervous system therapeutics.

Synthetic methodologies for CAS 36660-46-5 continue to evolve, with recent publications describing improved green chemistry approaches and catalytic processes. The compound's preparation typically involves naphthalene functionalization followed by amide bond formation, with modern techniques emphasizing atom economy and reduced environmental impact. These advancements address the chemical industry's shift toward sustainable synthesis and green pharmaceutical manufacturing.

Analytical characterization of 2-(naphthalen-2-yl)acetamide employs advanced techniques including NMR spectroscopy, mass spectrometry, and X-ray crystallography. The compound's crystalline properties have attracted attention in materials science, particularly for understanding molecular packing and intermolecular interactions. These studies contribute to broader research in crystal engineering and pharmaceutical solid-state chemistry.

From a commercial perspective, 36660-46-5 serves as an important fine chemical intermediate for various industries. Suppliers and manufacturers are responding to increased demand by developing high-purity grades suitable for research and development applications. The market for naphthalene derivatives continues to expand, driven by innovations in medicinal chemistry and functional materials.

Recent patent literature reveals growing intellectual property activity surrounding 2-(naphthalen-2-yl)acetamide derivatives, particularly in areas of therapeutic applications and material innovations. This trend reflects the compound's versatility and the pharmaceutical industry's ongoing search for novel chemical entities with improved pharmacological properties.

Quality control standards for CAS No. 36660-46-5 have become more stringent, with analytical methods now capable of detecting impurities at parts-per-million levels. This advancement supports the compound's use in preclinical research and drug development pipelines, where chemical purity is critical for reliable biological evaluation.

Environmental and safety assessments of 2-(naphthalen-2-yl)acetamide continue to inform proper handling procedures. While not classified as hazardous under standard conditions, researchers emphasize responsible laboratory practices when working with organic compounds. These considerations align with broader industry commitments to chemical safety and responsible research practices.

The future research directions for 36660-46-5 appear promising, with ongoing investigations into its structure-property relationships and potential applications in emerging technologies. As synthetic methodologies advance and biological evaluations progress, this compound may play increasingly important roles in both pharmaceutical development and advanced material science.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:36660-46-5)2-(naphthalen-2-yl)acetamide
A1159362
Purity:99%
Quantity:1g
Price ($):276.0
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