Cas no 143773-13-1 (1-(Pyridin-2-yl)nonan-1-one)

1-(Pyridin-2-yl)nonan-1-one is a ketone derivative featuring a pyridine moiety at the 2-position, offering a unique combination of lipophilic and aromatic properties. This compound is characterized by its nine-carbon alkyl chain, which enhances solubility in organic solvents while maintaining reactivity typical of pyridine-containing structures. Its molecular structure makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and coordination chemistry. The pyridinyl group facilitates chelation with metal ions, while the ketone functionality allows for further derivatization. This compound is valued for its stability and potential applications in catalytic systems and ligand design.
1-(Pyridin-2-yl)nonan-1-one structure
1-(Pyridin-2-yl)nonan-1-one structure
Product Name:1-(Pyridin-2-yl)nonan-1-one
CAS No:143773-13-1
MF:C14H21NO
MW:219.322643995285
MDL:MFCD00966398
CID:1032064
PubChem ID:3845398
Update Time:2025-05-22

1-(Pyridin-2-yl)nonan-1-one Chemical and Physical Properties

Names and Identifiers

    • 1-(Pyridin-2-yl)nonan-1-one
    • 1-(Pyridin-2-yl)non-1-one
    • 1-pyridin-2-ylnonan-1-one
    • 2-Nonanoylpyridine
    • DTXSID20397222
    • AKOS011914486
    • 143773-13-1
    • 1-Nonanone, 1-(2-pyridinyl)-
    • 2-pyridyl octyl ketone
    • MFCD00966398
    • SCHEMBL1254914
    • MDL: MFCD00966398
    • Inchi: 1S/C14H21NO/c1-2-3-4-5-6-7-11-14(16)13-10-8-9-12-15-13/h8-10,12H,2-7,11H2,1H3
    • InChI Key: MBWBQWMBPVFJCV-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CN=1)CCCCCCCC

Computed Properties

  • Exact Mass: 219.16200
  • Monoisotopic Mass: 219.162314293g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 8
  • Complexity: 191
  • 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: 4.4
  • Topological Polar Surface Area: 30?2

Experimental Properties

  • PSA: 29.96000
  • LogP: 4.01490

1-(Pyridin-2-yl)nonan-1-one Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1-(Pyridin-2-yl)nonan-1-one Pricemore >>

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Additional information on 1-(Pyridin-2-yl)nonan-1-one

1-(Pyridin-2-yl)nonan-1-one (CAS No. 143773-13-1): A Comprehensive Overview of Properties and Applications

1-(Pyridin-2-yl)nonan-1-one (CAS No. 143773-13-1) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, agrochemical development, and material science. This compound, characterized by its unique pyridine moiety and ketone functional group, serves as a versatile intermediate in synthetic chemistry. Researchers and industry professionals frequently search for terms like "1-(Pyridin-2-yl)nonan-1-one synthesis", "CAS 143773-13-1 applications", and "pyridinyl ketone derivatives", highlighting its relevance in modern chemical innovation.

The molecular structure of 1-(Pyridin-2-yl)nonan-1-one combines a nine-carbon alkyl chain with a pyridine-2-yl group, making it an interesting subject for studies on lipophilicity and bioavailability. Recent trends in drug discovery emphasize the importance of such hybrid molecules, particularly in the design of CNS-targeting compounds and enzyme inhibitors. With growing interest in AI-assisted molecular design, this compound has been featured in several computational chemistry studies exploring structure-activity relationships (SAR) for various therapeutic targets.

In the pharmaceutical sector, 1-(Pyridin-2-yl)nonan-1-one has shown promise as a building block for kinase inhibitors and GPCR modulators. The compound's balanced hydrophobic-hydrophilic properties make it particularly valuable for optimizing drug candidates' ADME profiles. Current research focuses on its potential in developing treatments for neurodegenerative diseases and metabolic disorders, aligning with the global healthcare community's priorities.

The agrochemical industry has also explored applications of CAS 143773-13-1 in developing novel plant growth regulators and pest control agents. Its structural features contribute to improved systemic movement in plants and enhanced target specificity, addressing the growing demand for sustainable agriculture solutions. Recent patents highlight its use in formulations that minimize environmental impact while maintaining efficacy.

From a synthetic chemistry perspective, 1-(Pyridin-2-yl)nonan-1-one serves as an excellent example of heterocyclic ketone chemistry. Modern green chemistry approaches have developed more efficient routes to this compound, reducing waste and energy consumption. These advancements respond to the chemical industry's push toward sustainable manufacturing practices, a topic of increasing importance in regulatory and consumer circles.

Material scientists have investigated pyridinyl ketone derivatives like 143773-13-1 for their potential in organic electronics and coordination chemistry. The compound's ability to form stable complexes with various metals makes it valuable for creating advanced materials with tailored optical and electronic properties. This aligns with current research trends in energy storage and optoelectronic devices.

The global market for 1-(Pyridin-2-yl)nonan-1-one reflects its growing importance across multiple industries. Suppliers and manufacturers frequently list this compound under categories such as "pharmaceutical intermediates", "research chemicals", and "specialty chemicals". Quality standards for CAS 143773-13-1 typically require high purity levels (>98%), with strict controls on impurities that could affect downstream applications.

Analytical characterization of 1-(Pyridin-2-yl)nonan-1-one typically involves techniques like HPLC, GC-MS, and NMR spectroscopy. These methods ensure proper identification and quantification, crucial for research and industrial applications. Recent advancements in analytical chemistry have improved the detection limits and accuracy for such compounds, supporting quality control in various applications.

Safety considerations for handling 143773-13-1 follow standard laboratory protocols for organic compounds. While not classified as hazardous under normal conditions, proper personal protective equipment (PPE) and ventilation are recommended when working with this material. These precautions align with the broader chemical industry's commitment to workplace safety and responsible chemical management.

Future research directions for 1-(Pyridin-2-yl)nonan-1-one may explore its potential in catalysis, supramolecular chemistry, and nanotechnology. The compound's versatility makes it a candidate for developing smart materials and responsive systems, areas of intense scientific interest. As synthetic methodologies advance, we anticipate new discoveries about this compound's capabilities and applications.

For researchers seeking 1-(Pyridin-2-yl)nonan-1-one suppliers, it's essential to verify certificates of analysis and compliance with relevant quality standards. The compound's increasing importance in various fields has led to expanded availability from specialty chemical providers worldwide. Proper storage conditions typically recommend protection from moisture and extreme temperatures to maintain stability.

In conclusion, CAS 143773-13-1 represents a fascinating case study in modern chemical research and development. Its applications span from drug discovery to advanced materials, reflecting the interdisciplinary nature of contemporary science. As research continues to uncover new properties and uses for 1-(Pyridin-2-yl)nonan-1-one, this compound will likely remain an important tool for scientists and engineers across multiple disciplines.

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