13909-73-4 Usage
Description
2',3',4'-Trimethoxyacetophenone is an organic compound characterized by its clear yellow liquid appearance. It is known for its reactivity with BCl3, which results in the formation of the corresponding 2,3-dihydroxy-4-methoxy compounds.
Uses
Used in Chemical Synthesis:
2',3',4'-Trimethoxyacetophenone is used as a key intermediate in the synthesis of various organic compounds. Its ability to react with BCl3 and form 2,3-dihydroxy-4-methoxy compounds makes it a valuable building block for creating a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2',3',4'-Trimethoxyacetophenone is used as a starting material for the development of new drugs. Its unique chemical properties allow for the creation of novel drug candidates with potential therapeutic benefits.
Used in Dye and Pigment Industry:
2',3',4'-Trimethoxyacetophenone is used as a precursor in the production of dyes and pigments. Its reactivity and versatility make it a valuable component in the synthesis of various colorants used in the textile, paint, and printing industries.
Used in Flavor and Fragrance Industry:
2',3',4'-Trimethoxyacetophenone is used as a building block for the creation of unique fragrances and flavors. Its chemical properties allow for the development of new scents and tastes that can be used in the perfume, cosmetics, and food industries.
Used in Material Science:
In the field of material science, 2',3',4'-Trimethoxyacetophenone is used in the development of advanced materials with specific properties. Its reactivity and ability to form various compounds make it a useful component in the creation of new polymers, coatings, and other materials with unique characteristics.
Preparation
Obtained by reaction of dimethyl sulfate with gallacetophenone in methanol in the presence of potassium hydroxide.
Check Digit Verification of cas no
The CAS Registry Mumber 13909-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,0 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13909-73:
(7*1)+(6*3)+(5*9)+(4*0)+(3*9)+(2*7)+(1*3)=114
114 % 10 = 4
So 13909-73-4 is a valid CAS Registry Number.
13909-73-4Relevant articles and documents
An unusual anodic methoxylation: 3,4-dimethoxyacetophenone
Hawkes,Hawkes,Comninos,Pardini,Viertler
, p. 8133 - 8136 (1992)
The electrolysis of 3,4-dimethoxyacetophenone in methanol at a platinum anode gives a high yield of 1-acetyl-4,5,5,6-tetramethoxycyclohexa-1,3-diene, whose structure is proven by 1H and 13C NMR.
Novel 2,4,5-trisubstituted oxazole derivatives: Synthesis and antiproliferative activity
Liu, Xin-Hua,Lv, Peng-Cheng,Xue, Jia-Yu,Song, Bao-An,Zhu, Hai-Liang
experimental part, p. 3930 - 3935 (2009/12/04)
Microwave irradiation promotes the rapid O,N-acylation-cyclodehydration cascade reaction of oximes and acid chloride. Twenty novel 2,4,5-trisubstituted oxazole derivatives containing heterocycle moiety were synthesized and evaluated for their antiproliferative activity. The twenty compounds are all first reported and their structures were established by elemental analysis, 1H NMR and 13C NMR spectra. The bioassay tests showed that compounds 2-(2-(2-fluorophenyl)-4-(2,3,4-trimethoxyphenyl)oxazol-5-ylthio)benzo[d]thiazole (6af), 2-(2-(pyridin-3-yl)-4-(2,3,4-trimethoxyphenyl)oxazol-5-ylthio)pyrimidine (6bg) and 2-(2-(2-fluorophenyl)-4-(2,3,4-trimethoxyphenyl)oxazol-5-ylthio)-5-methyl-1,3,4-thiadiazole (6cf) displayed good antiproliferative activity in vitro, which were comparable to the positive control (5-fluorouracil).
FLAVONES
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Page/Page column 18; 49, (2008/06/13)
The present invention relates to flavone compounds and their use in methods of treating or preventing parasitic infections, fungal infections and cell proliferative disorders. The present invention also relates to the use of flavone compounds in methods of controlling pests.