Basic information Safety Supplier Related

7-METHOXY-2-NAPHTHOL

Basic information Safety Supplier Related

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
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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
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
8-9-23
HS Code 
29071990

MSDS

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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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