CAS 77301-42-9
:1-(6-Methoxy-2-naphthyl)ethanol
Description:
1-(6-Methoxy-2-naphthyl)ethanol, with the CAS number 77301-42-9, is an organic compound characterized by its naphthalene structure substituted with a methoxy group and an ethanol moiety. This compound typically exhibits a moderate polarity due to the presence of the hydroxyl (-OH) group, which can engage in hydrogen bonding, enhancing its solubility in polar solvents. The methoxy group contributes to its aromatic character and can influence its reactivity and interaction with biological systems. As a naphthalene derivative, it may exhibit interesting photophysical properties, including fluorescence, which can be useful in various applications such as dyes or sensors. The compound's structural features suggest potential uses in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with naphthalene derivatives. However, specific properties such as melting point, boiling point, and spectral data would require empirical measurement or literature reference for precise characterization.
Formula:C13H14O2
InChI:InChI=1S/C13H14O2/c1-9(14)10-3-4-12-8-13(15-2)6-5-11(12)7-10/h3-9,14H,1-2H3
InChI key:InChIKey=OUVJWFRUESFCCY-UHFFFAOYSA-N
SMILES:C(C)(O)C1=CC2=C(C=C(OC)C=C2)C=C1
Synonyms:- (1R)-1-(6-methoxynaphthalen-2-yl)ethanol
- (±)-1-(6-Methoxynaphthyl)ethanol
- 1-(6-Methoxynaphthalen-2-Yl)Ethanol
- 1-(6-Methoxynaphthalen-2-yl)ethan-1-ol
- 2-(1-Hydroxyethyl)-6-methoxynaphthalene
- 2-Naphtalenemethanol, 6-methoxy-.alpha.-methyl-
- 2-Naphthalenemethanol, 6-Methoxy-Alpha-Methyl-
- 2-Naphthalenemethanol, 6-methoxy-α-methyl-
- 6-Methoxy-α-methyl-2-naphthalenemethanol
- α-(6-Methoxy-2-naphthyl)ethanol
- α-(6-Methoxy-2-naphthyl)ethyl alcohol
- See more synonyms
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Found 15 products.
2-(1-Hydroxyethyl)-6-methoxynaphthalene
CAS:Formula:C13H14O2Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:202.251-(6-Methoxy-2-naphthyl)ethanol, 98%
CAS:<p>Racemic 1-(6-methoxy-2-naphthyl)ethanol converts to the methyl ester of naproxen. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item cod</p>Formula:C13H14O2Purity:98%Color and Shape:White to pale cream, PowderMolecular weight:202.25Naproxen Related Compound K (1-(6-Methoxynaphthalen-2-yl)ethanol)
CAS:<p>Ether-alcohols and their halogenated, sulfonated, nitrated or nitrosated derivatives, nesoi</p>Formula:C13H14O2Color and Shape:White Crystalline PowderMolecular weight:202.099381-(6-Methoxynaphthalen-2-yl)ethanol
CAS:Formula:C13H14O2Purity:98%Color and Shape:SolidMolecular weight:202.24911-(6-Methoxynaphthalen-2-yl)ethanol
CAS:<p>1-(6-Methoxynaphthalen-2-yl)ethanol</p>Purity:95%Molecular weight:202.25g/mol1-(6-Methoxy-2-naphthyl)ethanol
CAS:<p>1-(6-Methoxy-2-naphthyl)ethanol</p>Purity:≥98%Molecular weight:202.25g/molNaproxen EP Impurity K (Naproxen USP Related Compound K)
CAS:Formula:C13H14O2Color and Shape:White To Off-White SolidMolecular weight:202.25(1RS)-1-(6-Methoxynaphthalen-2-yl)ethanol
CAS:Controlled ProductFormula:C13H14O2Color and Shape:NeatMolecular weight:202.251-(6-Methoxy-2-naphthyl)ethanol
CAS:<p>1-(6-Methoxy-2-naphthyl)ethanol is used as pharmaceutical intermediates.</p>Formula:C13H14O2Purity:99.79%Color and Shape:SolidMolecular weight:202.25(1RS)-1-(6-Methoxy-2-naphthyl)ethanol (Naproxen Impurity K)
CAS:Controlled Product<p>Impurity Naproxen EP Impurity K<br>Applications Naproxen impurity K.<br>References Boynton, C., et al.: J. Clin. Pharmacol., 28, 512 (1988), Li, J., et al.: J. Med. Chem., 39, 1846 (1996), Monser, L., et al.: J. Pharm. Biomed. Anal., 27, 851 (2002),<br></p>Formula:C13H14O2Color and Shape:White To Light YellowMolecular weight:202.25(1RS)-1-(6-Methoxy-2-naphthyl)ethanol
CAS:<p>(1RS)-1-(6-Methoxy-2-naphthyl)ethanol is a multiphase test drug that exhibits reactive properties. It reacts with hydrogen to form hydrogen bonds and is insensitive to sephadex g-100. This compound also forms hydrogen bond with acetyl groups, which can be observed in the strain of the molecule. (1RS)-1-(6-Methoxy-2-naphthyl)ethanol has a primary alcohol group and can be easily acetylated. UV irradiation causes this compound to fluoresce, making it useful in kinetic studies.</p>Formula:C13H14O2Purity:Min. 95%Molecular weight:202.25 g/mol














