CAS 3588-80-5
:5-Methoxy-1-naphthalenol
Description:
5-Methoxy-1-naphthalenol, with the CAS number 3588-80-5, is an organic compound characterized by its naphthalene structure substituted with a methoxy group and a hydroxyl group. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the naphthalene core. The presence of the methoxy group enhances its solubility in organic solvents, while the hydroxyl group contributes to its potential as a phenolic compound, which can exhibit antioxidant properties. 5-Methoxy-1-naphthalenol is of interest in various fields, including organic synthesis and medicinal chemistry, due to its potential biological activities. Its reactivity can be influenced by the functional groups present, allowing for various chemical transformations. Additionally, this compound may be studied for its interactions in biological systems, particularly in relation to its effects on cellular processes. Safety data should be consulted for handling and usage, as with any chemical substance.
Formula:C11H10O2
InChI:InChI=1S/C11H10O2/c1-13-11-7-3-4-8-9(11)5-2-6-10(8)12/h2-7,12H,1H3
InChI key:InChIKey=WLZPYTDCBHITRF-UHFFFAOYSA-N
SMILES:O(C)C=1C2=C(C(O)=CC=C2)C=CC1
Synonyms:- 5-Methoxy-1-naphthalenol
- 1-Hydroxy-5-methoxynaphthalene
- 1-Naphthalenol, 5-methoxy-
- 1-Naphthol, 5-methoxy-
- 1,5-Naphthohydroquinone monomethyl ether
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Found 4 products.
5-METHOXYNAPHTHALEN-1-OL
CAS:Formula:C11H10O2Purity:95%+Color and Shape:SolidMolecular weight:174.1995-Methoxy-1-naphthalenol
CAS:Controlled Product<p>Applications 5-Methoxy-1-naphthalenol (cas# 3588-80-5) is a compound useful in organic synthesis.<br></p>Formula:C11H10O2Color and Shape:NeatMolecular weight:174.205-Methoxynaphthalen-1-ol
CAS:<p>5-Methoxynaphthalen-1-ol is an alkylating agent that has been shown to have hypoglycemic activity. It is a nonpolar solvent, which can be used for the extraction of alkaloids from plants and fungi. 5-Methoxynaphthalen-1-ol has been shown to bind specifically to the hydroxyl group of proteins, nucleic acids, and lipids. This binding inhibits the metabolism of carbohydrates and leads to an increase in blood sugar levels. 5-Methoxynaphthalen-1-ol is synthesized by reacting naphthalene with a mixture of nitric acid and hydrochloric acid in a polar solvent such as water or ethanol. The reaction produces dihydroxynaphthalenes, which are then oxidized with potassium permanganate in a nonpolar solvent such as benzene or chloroform.</p>Formula:C11H10O2Purity:Min. 95%Molecular weight:174.2 g/mol



