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1818-28-6

1818-28-6 Structure

1818-28-6 Structure
IdentificationBack Directory
[Name]

2',4',5'-TRIMETHOXYACETOPHENONE
[CAS]

1818-28-6
[Synonyms]

2,4,5-TRIMETHOXYACETOPHENONE
trimethyl(1-pyrazolyl)silane
2',4',5'-TRIMETHOXYACETOPHENONE
1-(2,4,5-Trimethoxyphenyl)ethanone
Acetophenone, 2',4',5'-trimethoxy-
Ethanone, 1-(2,4,5-trimethoxyphenyl)-
1-(2,4,5-trimethoxyphenyl)ethan-1-one
[EINECS(EC#)]

217-333-4
[Molecular Formula]

C11H14O4
[MDL Number]

MFCD00017237
[MOL File]

1818-28-6.mol
[Molecular Weight]

210.23
Chemical PropertiesBack Directory
[Melting point ]

98-102°C
[Boiling point ]

285-290 °C(Press: 33 Torr)
[density ]

1.089±0.06 g/cm3(Predicted)
[form ]

solid
[EPA Substance Registry System]

Ethanone, 1-(2,4,5-trimethoxyphenyl)- (1818-28-6)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

3
[TSCA ]

TSCA listed
Hazard InformationBack Directory
[Preparation]

Preparation by reaction of acetyl chloride with hydroxyhydroquinone trimethyl ether in the presence of aluminium chloride.
[Synthesis Reference(s)]

Journal of Medicinal Chemistry, 33, p. 1155, 1990 DOI: 10.1021/jm00166a012
[Synthesis]

2,4,5-Trimethoxy acetophenone is synthesised using 2-Hydroxy-4,5-dimethoxy acetophenone as raw material by chemical reaction. The specific synthesis steps are as follows:
2-Hydroxy-4,5-dimethoxyacetophenone(5 g,0.0255 mole) in dry acetone (100 ml)is refluxed for 30 hr under anhydrous conditions with dimethyl sulphate (2.8 ml,3.78 g,0.03 mole)and ignited potassium carbonate (20 g).The mixture is filtered and the inorganic residue washed with hot acetone (2 x 20 ml).The combined acetone solution is distilled and the oily residue macerated with crushed ice.The solid product is filtered,washed with water and dried.It is crystallised from benzene as colourless needles.Yield 4.5g (84.1%).M.p.97(lit.m.p.102).
2',4',5'-TRIMETHOXYACETOPHENONE synthesis
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