Cas no 1999-64-0 (6-Ethylnaphthalen-2-ol)

6-Ethylnaphthalen-2-ol is a substituted naphthalene derivative characterized by the presence of an ethyl group at the 6-position and a hydroxyl group at the 2-position of the naphthalene ring. This compound is of interest in organic synthesis and material science due to its aromatic structure and functional groups, which enable further chemical modifications. Its phenolic moiety offers reactivity in electrophilic substitution reactions, while the ethyl group may influence solubility and steric properties. Potential applications include intermediates for dyes, pharmaceuticals, or advanced polymers. The compound's stability and well-defined reactivity profile make it a useful building block in research and industrial chemistry.
6-Ethylnaphthalen-2-ol structure
6-Ethylnaphthalen-2-ol structure
Product Name:6-Ethylnaphthalen-2-ol
CAS No:1999-64-0
MF:C12H12O
MW:172.223083496094
MDL:MFCD07368645
CID:118284
PubChem ID:20541757
Update Time:2025-11-02

6-Ethylnaphthalen-2-ol Chemical and Physical Properties

Names and Identifiers

    • 6-Ethyl-2-naphthalenol
    • 6-Ethylnaphthalen-2-ol
    • 6-Ethyl-2-naphthol
    • 2,2'-Bipyridine, 6-ethyl-
    • 6-Aethyl-[2]naphthol
    • 6-ethyl-[2,2']bipyridinyl
    • 6-ethyl-[2]naphthol
    • 6-ethyl-2,2'-bipyridine
    • 6-Hydroxy-2-aethyl-naphthalin
    • CTK2B0152
    • 6-Ethyl-naphthalen-2-ol
    • 2-Ethyl-6-naphthol
    • 2-Naphthalenol,6-ethyl-(9CI)
    • 2-Naphthalenol, 6-ethyl-
    • Jsp002634
    • FCH855224
    • AX8000785
    • ST24033106
    • SY108635
    • SCHEMBL2051891
    • AKOS006287708
    • MFCD07368645
    • FT-0633554
    • FT-0649474
    • 1999-64-0
    • BAA99964
    • DS-12647
    • 6-Ethyl-2-Naphthalol
    • A879896
    • 4-Pentene-1,2-dicarboxylicanhydride
    • CS-0061462
    • AC-16723
    • MDL: MFCD07368645
    • Inchi: 1S/C12H12O/c1-2-9-3-4-11-8-12(13)6-5-10(11)7-9/h3-8,13H,2H2,1H3
    • InChI Key: UMFMPNDTINUJER-UHFFFAOYSA-N
    • SMILES: OC1C=CC2C=C(C=CC=2C=1)CC

Computed Properties

  • Exact Mass: 172.08886
  • Monoisotopic Mass: 172.088815002g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 167
  • 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: 3.6
  • Topological Polar Surface Area: 20.2

Experimental Properties

  • Density: 1.112±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 98 oC
  • Boiling Point: 322.3 °C at 760 mmHg
  • Flash Point: 155.4 °C
  • Solubility: Almost insoluble (0.053 g/l) (25 o C),
  • PSA: 20.23

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6-Ethylnaphthalen-2-ol Suppliers

Amadis Chemical Company Limited
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(CAS:1999-64-0)6-Ethylnaphthalen-2-ol
Order Number:A879896
Stock Status:in Stock
Quantity:1g/5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 10:02
Price ($):151.0/364.0

6-Ethylnaphthalen-2-ol Related Literature

Additional information on 6-Ethylnaphthalen-2-ol

6-Ethylnaphthalen-2-ol (CAS No. 1999-64-0): Properties, Applications, and Market Insights

6-Ethylnaphthalen-2-ol (CAS No. 1999-64-0) is a specialized organic compound belonging to the naphthalene derivatives family. This compound is increasingly gaining attention in the chemical and pharmaceutical industries due to its unique structural properties and versatile applications. With the growing demand for high-performance intermediates in organic synthesis, 6-Ethylnaphthalen-2-ol has emerged as a valuable building block for various advanced materials and bioactive molecules.

The molecular structure of 6-Ethylnaphthalen-2-ol features an ethyl group at the 6-position and a hydroxyl group at the 2-position of the naphthalene ring. This configuration imparts distinct chemical reactivity and solubility characteristics, making it particularly useful in fine chemical synthesis. Recent studies have explored its potential as a precursor for fluorescent materials and pharmaceutical intermediates, aligning with current research trends in functional organic compounds.

One of the most significant applications of 6-Ethylnaphthalen-2-ol is in the development of advanced materials. Researchers are investigating its use in creating organic semiconductors and photovoltaic materials, which are crucial for next-generation renewable energy technologies. The compound's ability to form stable π-conjugated systems makes it particularly interesting for optoelectronic applications, a hot topic in materials science today.

In the pharmaceutical sector, 6-Ethylnaphthalen-2-ol serves as a key intermediate for synthesizing various bioactive compounds. Its structural features allow for modifications that can lead to molecules with potential therapeutic properties. Current research is exploring its derivatives for possible anti-inflammatory and antioxidant activities, addressing the growing consumer interest in health and wellness products.

The synthesis of 6-Ethylnaphthalen-2-ol typically involves Friedel-Crafts alkylation of naphthalene derivatives, followed by selective hydroxylation. Modern green chemistry approaches are being developed to improve the efficiency and sustainability of its production, responding to the industry's push for environmentally friendly processes. These advancements are particularly relevant given the current focus on sustainable chemical manufacturing.

From a market perspective, the demand for 6-Ethylnaphthalen-2-ol is expected to grow steadily, driven by its expanding applications in specialty chemicals and pharmaceutical research. The compound's niche applications in material science and drug development position it as a valuable product in the fine chemicals market. Industry analysts note increasing interest from both academic researchers and industrial manufacturers, particularly in regions with strong chemical innovation ecosystems.

Quality control is crucial when working with 6-Ethylnaphthalen-2-ol, with purity levels typically exceeding 98% for most research applications. Advanced analytical techniques such as HPLC and GC-MS are commonly employed to ensure product consistency. These quality standards are particularly important given the compound's use in high-value applications where precise molecular characteristics are essential.

Storage and handling of 6-Ethylnaphthalen-2-ol require standard laboratory precautions. The compound should be kept in airtight containers away from direct sunlight and moisture to maintain stability. These handling procedures align with general best practices for organic compounds and reflect the compound's relative stability under normal conditions.

Current research trends involving 6-Ethylnaphthalen-2-ol include exploring its potential in catalysis and supramolecular chemistry. Scientists are investigating how modifications to its structure might create novel molecular recognition systems or catalytic frameworks. These investigations are part of broader efforts to develop smart materials and advanced catalysts, areas that are receiving significant research funding worldwide.

For researchers and industry professionals seeking 6-Ethylnaphthalen-2-ol, it's important to source the compound from reputable suppliers who can provide comprehensive analytical data and technical specifications. The availability of detailed safety data sheets and certificates of analysis ensures proper handling and facilitates regulatory compliance, especially for users in regulated industries.

As the chemical industry continues to evolve, compounds like 6-Ethylnaphthalen-2-ol demonstrate how specialty chemicals can bridge the gap between fundamental research and practical applications. Its versatility across multiple disciplines makes it a compound worth watching in the coming years, particularly as new applications emerge in cutting-edge technologies and innovative material systems.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:1999-64-0)6-Ethylnaphthalen-2-ol
A879896
Purity:99%/99%
Quantity:1g/5g
Price ($):151.0/364.0
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