1078-19-9

  • Product Name:6-Methoxy-1-Tetralone
  • Molecular Formula:C11H12O2
  • Purity:99%
  • Molecular Weight:176.215
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Product Details;

CasNo: 1078-19-9

Molecular Formula: C11H12O2

Appearance: yellow crystalline powder

Quality Factory Supply Top Purity 6-Methoxy-1-Tetralone 1078-19-9 Lowest Price

  • Molecular Formula:C11H12O2
  • Molecular Weight:176.215
  • Appearance/Colour:yellow crystalline powder 
  • Vapor Pressure:0.000528mmHg at 25°C 
  • Melting Point:77-79 ºC 
  • Refractive Index:1.548 
  • Boiling Point:312.5 ºC at 760 mmHg 
  • Flash Point:153.4 ºC 
  • PSA:26.30000 
  • Density:1.124 g/cm3 
  • LogP:2.21420 

6-Methoxytetralone(Cas 1078-19-9) Usage

Chemical Properties

yellow to light brown fine crystalline powder

Uses

6-Methoxy-1-tetralone is a reagent useful in the synthesis of (2-(furanyl)vinyl)-1-tetralone chalcones which possesses anticancer agents and inducers of apoptosis.

Synthesis Reference(s)

Journal of the American Chemical Society, 64, p. 94, 1942 DOI: 10.1021/ja01253a025Tetrahedron Letters, 9, p. 2917, 1968 DOI: 10.1016/S0040-4039(00)89611-2

Synthesis

The synthesis of?6-methoxy-1-tetralone is as follows:Eaton's reagent (1.00 mL, 5.31 mmol) was added slowly to a stirred solution of methyl 4-(3-methoxyphenyl)butanoate (4; 0.37g, 1.78 mmol) in DCE (1 mL). The resulting mixture was stirred at 75 °C for 2h under N2 atmosphere. Then, the reaction mixture was allowed to reach room temperature, and was poured over ice-water and extracted with EtOAc (3 × 15 mL). The combined organic extracts were washed successively with brine (2 × 15 mL) and H2O (2 × 20 mL), filtered over Na2SO4 and concentrated under reduced pressure. The resulting brownish oil was fractionated by column chromatography (silica gel, EtOAc-hexanes, 1:9) to obtain 6-methoxy-1-tetralone as ayellowish oil; yield: 0.28 g (91%).

InChI:InChI=1/C11H12O2/c1-13-9-5-6-10-8(7-9)3-2-4-11(10)12/h5-7H,2-4H2,1H3

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1078-19-9 Process route

4-(m-methoxyphenyl)butanoic acid
24743-11-1

4-(m-methoxyphenyl)butanoic acid

8-methoxy-1-tetralone
13185-18-7

8-methoxy-1-tetralone

6-methoxy-3,4-dihydro-1(2H)-naphthalenone
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6-methoxy-3,4-dihydro-1(2H)-naphthalenone

Conditions
Conditions Yield
With polyphosphoric ester; In chloroform; for 7h; Yield given. Yields of byproduct given; Ambient temperature;
 
6-methoxy-1,2,3,4-tetrahydronaphthalene
1730-48-9

6-methoxy-1,2,3,4-tetrahydronaphthalene

2-Methoxynaphthalene
93-04-9

2-Methoxynaphthalene

6-methoxy-3,4-dihydro-1(2H)-naphthalenone
1078-19-9

6-methoxy-3,4-dihydro-1(2H)-naphthalenone

Conditions
Conditions Yield
With dipotassium peroxodisulfate; copper(I) sulfate; In water; acetonitrile; at 65 - 70 ℃; for 3h;
10%
45%

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