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4-Acetyl-2,5-dihydroxy-2-methyl-2,3-dihydro-benzofuran-3-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109746-54-5

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109746-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109746-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,4 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109746-54:
(8*1)+(7*0)+(6*9)+(5*7)+(4*4)+(3*6)+(2*5)+(1*4)=145
145 % 10 = 5
So 109746-54-5 is a valid CAS Registry Number.

109746-54-5Downstream Products

109746-54-5Relevant academic research and scientific papers

Synthesis and Characteristics of Fluorinated Benzofurans

Kucklaender, Uwe,Herweg-Wahl, Ute,Poll, Wolfgang,Rickerich, Lutz

, p. 1841 - 1846 (2007/10/02)

Dihydrobenzofurans 4a-c and g-j were synthesized from 2-acetyl-1,4-benzoquinone (1) and β-diketones 2a-c and g-j and dehydrated to benzofurans 5a-i.The structure of 5d was examined by X-ray analysis.Reaction of quinone 9 and diketone 2g yielded directly fluorinated benzofurans 11a and 12b.The abnormal 1H-NMR spectra of benzofurans 5d, f and 11a are discussed.Formation of ketone hydrates 12a, b and 13 was detected.

Addition of β-Dicarbonyl Compounds to 2-Acetyl-p-benzoquinone

Kucklaender, Uwe,Herweg-Wahl, Ute,Massa, Werner,Baum, Gerhard

, p. 1791 - 1796 (2007/10/02)

The structure of adducts from 2-acetyl-p-benzoquinone (1) and acetoacetates 2a,b is corrected to dihydrobenzofuran derivatives 4a,b.The product from 1 and hexafluoroacetylacetone 5 is examined spectroscopically and by X-ray structure analysis, its structure is cleared up as cycloadduct 6.In solution fast rearrangement of 6 to dihydrobenzofuran 13 is observed.Reaction of 13 with acetyl chloride yields the monoacetate 12, treatment with aqueous acid is followed by cleavage to 14.In acetic acid tetralone derivative 16 is formed, which can be aromatized with acetic anhydride to naphthalene 17 and oxidized to naphthoquinone 18.

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