Cas no 176032-71-6 (Benzenamine, 3-(6-methoxy-2-naphthalenyl)-)

Benzenamine, 3-(6-methoxy-2-naphthalenyl)-, is a specialized aromatic amine compound featuring a naphthalene core substituted with a methoxy group at the 6-position and an aniline moiety at the 2-position. This structure imparts unique electronic and steric properties, making it valuable as an intermediate in organic synthesis, particularly for pharmaceuticals and advanced materials. Its conjugated system enhances stability and reactivity, facilitating applications in dye chemistry, ligand design, and polymer science. The methoxy group further improves solubility in organic solvents, aiding in synthetic manipulations. This compound is characterized by high purity and consistent performance, ensuring reliability in research and industrial processes.
Benzenamine, 3-(6-methoxy-2-naphthalenyl)- structure
176032-71-6 structure
Product Name:Benzenamine, 3-(6-methoxy-2-naphthalenyl)-
CAS No:176032-71-6
MF:C17H15NO
MW:249.307104349136
CID:1363688
PubChem ID:22724074
Update Time:2025-10-30

Benzenamine, 3-(6-methoxy-2-naphthalenyl)- Chemical and Physical Properties

Names and Identifiers

    • Benzenamine, 3-(6-methoxy-2-naphthalenyl)-
    • 3-(6-methoxynaphthalene-2-yl)phenylamine
    • 3-(6-Methoxynaphthalen-2-yl)aniline
    • 176032-71-6
    • GFHSOUYENFJHAU-UHFFFAOYSA-N
    • 3-(6-Methoxy-naphthalen-2-yl)-phenylamine
    • AKOS011240140
    • 3-(6-Methoxynaphthalene-2-yl)-phenylamine
    • SCHEMBL977907
    • MDL: MFCD08457017
    • Inchi: 1S/C17H15NO/c1-19-17-8-7-14-9-13(5-6-15(14)11-17)12-3-2-4-16(18)10-12/h2-11H,18H2,1H3
    • InChI Key: GFHSOUYENFJHAU-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC2=CC(=CC=C2C=1)C1C=CC=C(C=1)N

Computed Properties

  • Exact Mass: 249.11545
  • Monoisotopic Mass: 249.115364102g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 2
  • Complexity: 293
  • 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: 4.1
  • Topological Polar Surface Area: 35.2?2

Experimental Properties

  • PSA: 35.25

Benzenamine, 3-(6-methoxy-2-naphthalenyl)- Pricemore >>

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Additional information on Benzenamine, 3-(6-methoxy-2-naphthalenyl)-

Comprehensive Overview of Benzenamine, 3-(6-methoxy-2-naphthalenyl)- (CAS No. 176032-71-6)

Benzenamine, 3-(6-methoxy-2-naphthalenyl)-, with the CAS number 176032-71-6, is a specialized organic compound that has garnered significant attention in pharmaceutical and material science research. This compound, often referred to by its systematic name, belongs to the class of aromatic amines and naphthalene derivatives. Its unique molecular structure, combining a methoxy-naphthalene moiety with an aniline group, makes it a valuable intermediate in the synthesis of more complex molecules. Researchers and industries are increasingly exploring its potential applications, particularly in drug development and advanced material design.

One of the key reasons for the growing interest in Benzenamine, 3-(6-methoxy-2-naphthalenyl)- is its role as a precursor in the synthesis of bioactive compounds. Recent studies have highlighted its utility in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other therapeutic agents. The methoxy group and naphthalene ring in its structure contribute to its ability to interact with biological targets, making it a promising candidate for further pharmacological investigations. Additionally, its stability and solubility properties are being optimized for better performance in various formulations.

In the realm of material science, CAS 176032-71-6 is being studied for its potential in creating organic semiconductors and photovoltaic materials. The compound's conjugated system allows for efficient electron transfer, which is crucial for applications in OLEDs (organic light-emitting diodes) and solar cells. As the demand for sustainable and energy-efficient technologies rises, this compound could play a pivotal role in advancing green energy solutions. Researchers are also investigating its use in fluorescent dyes and sensors, leveraging its optical properties for high-performance applications.

From a synthetic chemistry perspective, the preparation of Benzenamine, 3-(6-methoxy-2-naphthalenyl)- involves multi-step reactions, often starting from 6-methoxy-2-naphthaldehyde or related intermediates. Optimizing these synthetic routes is a hot topic among chemists, as it impacts the compound's yield, purity, and scalability. Recent advancements in catalysis and green chemistry have enabled more efficient production methods, reducing environmental impact and costs. These innovations align with the broader industry trend toward sustainable and eco-friendly chemical processes.

The safety and handling of 176032-71-6 are also critical considerations for researchers and manufacturers. While the compound is not classified as hazardous under standard regulations, proper laboratory practices must be followed to ensure safe usage. Material Safety Data Sheets (MSDS) provide detailed guidelines on storage, handling, and disposal, emphasizing the importance of working in well-ventilated areas and using appropriate personal protective equipment (PPE). These precautions are essential to maintain a safe research environment and comply with regulatory standards.

Looking ahead, the future of Benzenamine, 3-(6-methoxy-2-naphthalenyl)- appears bright, with ongoing research uncovering new applications and improving existing ones. Its versatility and unique properties position it as a compound of interest across multiple disciplines, from medicine to renewable energy. As scientific communities continue to explore its potential, we can expect to see more innovations and breakthroughs leveraging this remarkable molecule. For those interested in the latest developments, staying updated with peer-reviewed journals and patent filings is highly recommended.

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