6,7-Dimethoxy-1-tetralone
6,7-Dimethoxy-1-tetralone Basic information
- Product Name:
- 6,7-Dimethoxy-1-tetralone
- Synonyms:
-
- 6,7-DIMETHOXY-1-TETRALONE
- 6,7-DIMETHOXY-1-TETRALONE, 97%%
- 6,7-Dimethoxy-3,4-dihydro-2H-naphthalen-1-one
- 6,7-dimethoxytetralin-1-one
- 4-dihydro-6
- 7-diMethoxy-
- 6,7-diMethoxy-3,4-dihydronaphthalen-1(2H)-one
- 6,7-Dimethoxy-1-tetralone 97%
- CAS:
- 13575-75-2
- MF:
- C12H14O3
- MW:
- 206.24
- Product Categories:
-
- C11 to C12
- Carbonyl Compounds
- Ketones
- Mol File:
- 13575-75-2.mol
6,7-Dimethoxy-1-tetralone Chemical Properties
- Melting point:
- 98-100 °C(lit.)
- Boiling point:
- 358.3±42.0 °C(Predicted)
- Density
- 1.140±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- Crystalline Powder or Crystals
- color
- White to off-white
- CAS DataBase Reference
- 13575-75-2(CAS DataBase Reference)
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
6,7-Dimethoxy-1-tetralone Usage And Synthesis
Uses
6,7-Dimethoxy-1-tetralone was used in the synthesis of 2-bromotetralones by undergoing bromination. It was also used as a precursor to quinolines with dopaminergic activity, naphthols with anti-inflammatory activity and benzophenanthridine alkaloids with antitumor activity.
Synthesis Reference(s)
Tetrahedron Letters, 24, p. 2939, 1983 DOI: 10.1016/S0040-4039(00)88063-6
General Description
6,7-Dimethoxy-1-tetralone reacts with 2-amino-4,5-dimethoxyacetophenone to form 5,6-dihydro-2,3,9,10-tetramethoxybenz[c]acridine.
Synthesis
13575-74-1
13575-75-2
General procedure for the synthesis of 6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one from 4-(3,4-dimethoxyphenyl)butyric acid: polyphosphoric acid (210 g) was added to a solution of dichloromethane (50 mL) in which 4-(3,4-dimethoxyphenyl)butyric acid (0.19 mol, 42 g) was dissolved, and the mixture was heated for 2 hr under reflux conditions. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the residue was slowly poured into crushed ice. The pH of the solution was adjusted to 7-8 with alkali, and the precipitate precipitated was filtered and dried to give 6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one (36 g, 93.3% yield) as a white solid with a melting point of 94-96 °C (literature value: 96-98 °C).1H NMR (400 MHz, CDCl3): δ 7.51 (s, 1H), 6.67 (s 1H), 3.93 (s, 3H), 3.91 (s, 3H), 2.89 (t, J=6Hz, 2H), 2.60 (t, J=6.4Hz, 2H), 2.15-2.09 (m, 2H); 13C NMR (101MHz, CDCl3): δ197.10, 153.51, 147.96, 139.27 125.79, 110.22, 108.57, 55.98, 38.50, 29.44, 23.61.
References
[1] Synthetic Communications, 2009, vol. 39, # 15, p. 2664 - 2673
[2] Journal of Organic Chemistry, 1985, vol. 50, # 24, p. 4933 - 4938
[3] European Journal of Medicinal Chemistry, 2012, vol. 53, p. 52 - 63
[4] Pharmazie, 1981, vol. 36, # 2, p. 88 - 91
[5] Tetrahedron Letters, 2009, vol. 50, # 13, p. 1407 - 1410
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6,7-Dimethoxy-1-tetralone(13575-75-2)Related Product Information
- Dimethyldimethoxysilane
- 1,1-Dimethoxyethane
- 1-Tetralone
- 1,2,3,4-Tetrahydronaphthalene
- Naphthalene
- 1,8-Naphthalic anhydride
- Dimethoxymethane
- 6-Hydroxy-1-tetralone
- 7-Hydroxy-1-tetralone
- 6-methoxy-1-tetralone
- 6,7-DIMETHOXY-2-TETRALONE
- 7-Methoxy-1-tetralone
- 6-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE
- 5 8-DIMETHOXY-1-TETRALONE 99
- 6,8-Dimethoxyl-2-tetralone
- 5,8-dimethoxy-2-tetralone
- 6-METHYLISOVANILLIN
- 1-(4,5-DIMETHOXY-2-METHYLPHENYL)ETHAN-1-ONE