6170-06-5

Usage

Uses

Used in Textile Industry:
Alizarin 1-methyl ether is used as a red dye for coloring fabrics, due to its vibrant color and compatibility with various textile materials.
Used in Ink Production:
It serves as a colorant in the production of inks, providing a consistent and long-lasting red hue for printing applications.
Used in Paint Industry:
Alizarin 1-methyl ether is utilized as a pigment in paints to impart a rich red color, enhancing the aesthetic appeal of painted surfaces.
Used in Other Colorant Applications:
alizarin 1-methyl ether is also employed in various other colorant applications, such as in the production of cosmetics, plastics, and paper, where its colorfast properties and stability contribute to the final product's quality.

InChI:InChI=1/C15H10O4/c1-19-15-11(16)7-6-10-12(15)14(18)9-5-3-2-4-8(9)13(10)17/h2-7,16H,1H3

Upstream product

• 186581-53-3 diazomethane 
• 75697-69-7 1-hydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl benzoate 
• 17205-33-3 2-acetoxy-3-chloro-1,4-naphthoquinone 
• 22516-62-7 2-(benzyloxy)-1-hydroxyanthracene-9,10-dione 
• 72-48-0 1,2-dihydroxy-9,10-anthracenedione 
• 54125-02-9 danishefsky's diene 
• 102468-63-3 2-benzyloxy-1-methoxy-anthraquinone 

Downstream Products

• 6003-12-9 alizarin dimethyl ether 
• 72-48-0 1,2-dihydroxy-9,10-anthracenedione 

Relevant academic research and scientific papers

Synthesis of proposed structure of rennellianone B: A study on rearrangement of anthraquinonyl propargyl ether toward 2H-pyranoanthraquinone

Rennellianone B was originally reported as a natural 2H-pyranoanthraquinone, isolated from the root of Rennellia elliptica Korth. An efficient synthesis of the proposed structure of rennellianone B was accomplished, starting from alizarin. The key feature of the synthesis involves the Claisen rearrangement of the anthraquinonyl propargyl ether intermediate to provide a 2H-pyranoanthraquinone moiety. In addition, intensive studies on rearrangement reaction conditions of anthraquinonyl propargyl ether toward the 2H-pyranoanthraquinone skeleton were described.

Reaction of 2-acetoxy-3-chloro and 2,3-diacetoxy naphthoquinones with 1,3-dioxy and 1,1,3-trioxy butadienes

Reaction of 2-acetoxy-3-chloro naphthoquinones towards the 1,3-dioxy diene (2) and the 1,1,3-trioxy diene (9) was examined. The competing influence of the acetoxy and chloro substituents was assessed from the regiochemistry of the resulting Diels-Alder ch