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6-Methoxy-3-methyl-1,7,8-trihydroxy-9,10-anthraquinone is a naturally occurring chemical compound that belongs to the anthraquinone family. It is found in various plants, including the Chinese herb rhubarb, and is known for its antioxidant, antimicrobial, anti-inflammatory, anticancer, and hepatoprotective properties.

7213-59-4

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7213-59-4 Usage

Uses

Used in Pharmaceutical Industry:
6-Methoxy-3-methyl-1,7,8-trihydroxy-9,10-anthraquinone is used as a potential candidate for the development of new pharmaceutical drugs due to its various health benefits, such as antioxidant, antimicrobial, anti-inflammatory, anticancer, and hepatoprotective properties.
Used in Textile Industry:
6-Methoxy-3-methyl-1,7,8-trihydroxy-9,10-anthraquinone is used as a dye in the textile industry because of its vibrant red color.

Check Digit Verification of cas no

The CAS Registry Mumber 7213-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7213-59:
(6*7)+(5*2)+(4*1)+(3*3)+(2*5)+(1*9)=84
84 % 10 = 4
So 7213-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O6/c1-6-3-7-11(9(17)4-6)15(20)12-8(13(7)18)5-10(22-2)14(19)16(12)21/h3-5,17,19,21H,1-2H3

7213-59-4Downstream Products

7213-59-4Relevant academic research and scientific papers

Reactions of Ketene Acetals. 13. Synthesis of Contiguously Trihydroxylated Naphto- and Anthraquinones

Roberge, Guy,Brassard, Paul

, p. 4161 - 4166 (2007/10/02)

A regiospecific method of obtaining various quinones bearing at least three adjacent hydroxyl groups has been devised by using a new vinylketene acetal, 2-methoxy-1,1,3-tris(trimethylsiloxy)-1,3-butadiene (9b).In this way the first total syntheses of dermoglaucin (50) and ceroalbolinic acid, as its pentamethyl derivative 49, have been achieved.The structure of another natural product, capareolatin dimethyl ether, was established indirectly by the unambiguous formation of one of the two possible isomers.Advantageous preparations of "7-hydroxyemodin", copareolatin, and isoerythrolaccin derivatives 32,38, and 2, as well as those of useful intermediates such as 2- and 3-chloro-5,7-dihydroxy-6-methoxynaphthoquinones or their dimethyl ethers, are described.

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