7-METHOXY-2-NAPHTHOL
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-methoxynaphthalen-2-ol
- 7-METHOXY-2-NAPHTHOL
- 7-Methoxy-2-naphthol, 97%, 97%
- 7-Methoxy-2-naphthol 98%
- CAS:
- 5060-82-2
- MF:
- C11H10O2
- MW:
- 174.2
- 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 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
- pka
- 9.45±0.40(Predicted)
- form
- Crystalline Powder or Chunks
- color
- White to brown
- BRN
- 2207279
MSDS
- Language:English Provider:SigmaAldrich
7-METHOXY-2-NAPHTHOL Usage And Synthesis
Chemical Properties
White to brown solid
Uses
7-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 Description
7-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
582-17-2
77-78-1
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
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7-METHOXY-2-NAPHTHOL(5060-82-2)Related Product Information
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