7-Methoxy-2-naphthol

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7-Methoxy-2-naphthol Basic information
Product Name:7-Methoxy-2-naphthol
Synonyms:2-Hydroxy-7-methoxynaphthalene;3-Methoxy-6-naphthol;7-Methoxy-2-naphthalenol;7-Methoxy-beta-naphthol;7-Methoxy-2-naphthol, 97%, 97%;7-Methoxy-2-naphthol 98%;7-METHOXY-2-PHTHOL;2-Naphthalenol, 7-methoxy-
CAS:5060-82-2
MF:C11H10O2
MW:174.2
EINECS:
Product Categories:Organic Building Blocks;Oxygen Compounds;Phenols;Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
Mol File:5060-82-2.mol
7-Methoxy-2-naphthol Structure
7-Methoxy-2-naphthol Chemical Properties
Melting point 116-119 °C(lit.)
Boiling point 336.7±15.0 °C(Predicted)
density 1.193
storage temp. Sealed in dry,Room Temperature
pka9.45±0.40(Predicted)
form Crystalline Powder or Chunks
color White to brown
BRN 2207279
InChI1S/C11H10O2/c1-13-11-5-3-8-2-4-10(12)6-9(8)7-11/h2-7,12H,1H3
InChIKeyUNFNRIIETORURP-UHFFFAOYSA-N
SMILESCOc1ccc2ccc(O)cc2c1
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
F 8-9-23
HS Code 29071990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
7-Methoxy-2-naphthol Usage And Synthesis
Chemical PropertiesWhite to brown solid
Uses7-Methoxy-2-naphthol may be used in the synthesis of new 1H-benzo[f]chromene derivatives. It may be used in the synthesis of 7-methoxy-2-naphthyl (MN)-derived xylosides in which the methoxy group served as a marker for NMR characterization and UV detection.
General Description7-Methoxy-2-naphthol is a 7-substituted-2-naphthol. Crystal structure of 7-methoxy-2-naphthol has been reported. Reaction of 7-methoxy-2-naphthol with N-methyl-N-phenylhydrazine under thermal conditions has been reported.
Synthesis
2,7-Dihydroxynaphthalene

582-17-2

Dimethyl sulfate

77-78-1

7-METHOXY-2-NAPHTHOL

5060-82-2

General method: a mixture of 2,7-dihydroxynaphthalene (500 mg, 2.64 mmol), dimethyl sulfate (0.5 ml, 5.3 mmol) and potassium carbonate (73.1 mg, 5.3 mmol) in acetonitrile (10 ml) was refluxed for 1 hour. After completion of the reaction, the solvent was removed by evaporation and the residue was poured into water and extracted with ethyl acetate. The organic layer was washed sequentially with water and brine, dried over anhydrous magnesium sulfate and subsequently concentrated under vacuum. The crude product was purified by silica gel column chromatography to afford 7-methoxy-2-naphthol using hexane/ethyl acetate (15:1) as eluent.

References[1] Molecular Pharmacology, 2013, vol. 84, # 5, p. 726 - 735
[2] Patent: US2006/52378, 2006, A1. Location in patent: Page/Page column 112
[3] Journal fuer Praktische Chemie (Leipzig), 1916, vol. <2> 94, p. 25
[4] Journal of medicinal chemistry, 1971, vol. 14, # 11, p. 1023 - 1026
7-Methoxy-2-naphthol Preparation Products And Raw materials
Raw materials2,7-Dihydroxynaphthalene-->Dimethyl sulfate-->Iodomethane-->Acetonitrile-->Potassium carbonate
Preparation Products2-Bromo-7-hydroxynaphthalene
Tag:7-Methoxy-2-naphthol(5060-82-2) Related Product Information
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