CAS 21388-17-0
:Naphthalene,2-ethyl-6-methoxy-
Description:
Naphthalene, 2-ethyl-6-methoxy- is an organic compound characterized by its structure, which includes a naphthalene backbone substituted with an ethyl group and a methoxy group. This compound is part of the polycyclic aromatic hydrocarbons family and exhibits properties typical of aromatic compounds, such as stability and a tendency to undergo electrophilic substitution reactions. It is generally a colorless to pale yellow solid at room temperature, with a characteristic odor reminiscent of mothballs, due to its structural similarity to naphthalene. The presence of the methoxy group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Naphthalene derivatives are often studied for their potential applications in organic synthesis, materials science, and as intermediates in the production of dyes and pharmaceuticals. Safety considerations include its potential toxicity and environmental impact, necessitating careful handling and disposal in laboratory and industrial settings.
Formula:C13H14O
Synonyms:- 2-Ethyl-6-methoxynaphthalene
- 2-Methoxy-6-ethylnaphthalene
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Found 9 products.
2-Ethylnerolin (2-Ethyl-6-methoxynaphthalene)
CAS:Aromatic ethers and their halogenated, sulfonated, nitrated or nitrosated derivativesFormula:C13H14OColor and Shape:Off-White SolidMolecular weight:186.104476-ETHYL-2-METHOXYLNAPHTHALINE
CAS:Formula:C13H14OPurity:98%Color and Shape:SolidMolecular weight:186.2497Naproxen EP Impurity J
CAS:Formula:C13H14OColor and Shape:White To Off-White SolidMolecular weight:186.252-Ethyl-6-methoxynaphthalene (Ethylnerolin)
CAS:Controlled ProductFormula:C13H14OColor and Shape:NeatMolecular weight:186.252-Ethyl-6-methoxynaphthalene
CAS:<p>2-Ethyl-6-methoxynaphthalene (2EMN) is a naproxen derivative that inhibits the enzyme cyclooxygenase and blocks the formation of prostaglandins. This compound is used in pharmaceutical preparations to treat pain and inflammation, as well as in mineralization studies. 2EMN binds to ferrite, forming a ternary complex, which leads to an increase in the rate of degradation of fatty acids. The experimental model for this reaction was found to be constant, with a high resistance against acidic or fatty acids.</p>Formula:C13H14OPurity:Min. 95%Molecular weight:186.25 g/mol









