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Usage

Uses

Used in Polymer and Resin Production:
5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate is used as a crosslinking agent for enhancing the stability and performance of various polymers and resins. Its ability to form strong covalent bonds with other molecules contributes to the improved mechanical properties and durability of the final products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate is used as a building block for the synthesis of certain drugs. Its unique structure and reactivity make it a valuable component in the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Adhesive and Coating Production:
5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate is used as a key component in the formulation of adhesives and coatings. Its strong bonding capabilities improve the adhesion and durability of these products, making them suitable for various applications, including automotive, construction, and consumer goods.
Used in Research and Development:
5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate is used as a research tool for creating new materials and chemical compounds. Its unique properties and reactivity make it a valuable asset in the development of innovative products and technologies across various industries.

InChI:InChI=1/C16H16O9/c1-8(17)22-7-13(21)12-5-14(23-9(2)18)16(25-11(4)20)15(6-12)24-10(3)19/h5-6H,7H2,1-4H3

Upstream product

• 97443-98-6 2-Chlor-1-(3,4,5-triacetoxyphenyl)ethanon 
• 108-24-7 acetic anhydride 
• 70475-59-1 3,4,5-triacetoxybenzoyl chloride 
• 64-19-7 acetic acid 
• 97443-97-5 2-Diazo-1-(3,4,5-triacetoxyphenyl)ethanon 
• 149-91-7 3,4,5-trihydroxybenzoic acid 
• 6635-24-1 3,4,5-triacetoxybenzoic acid 

Downstream Products

• 3020-09-5 3,7-dihydroxy-2-(3,4,5-trihydroxy-phenyl)-chromenylium; chloride 
• 528-53-0 delphinidin chloride 
• 178436-68-5 6-hydroxydelphinidin 

Relevant academic research and scientific papers

Synthesis of [4-14C]-pelargonidin chloride and [4- 14C]-delphinidin chloride

The synthesis of [4-14C]-pelargonidin chloride and [4- 14C]-delphinidin chloride via [formyl-14C]-2-(benzoyloxy)- 4,6-dihydroxybenzaldehyde, ω,4-diacetoxyacetophenone and ω,3,4,5-tetraacetoxyacetophenone is described. The first step comprised labelling of the carbonyl group of 2-(benzoyloxy)-4,6-dihydroxybenzaldehyde, verifying that the coupling with ω,4-diacetoxyacetophenone or ω,3,4,5-tetraacetoxyacetophenone under hydrogen chloride atmosphere resulted in the formation of [4-14C] labelled anthocyanidins. Copyright

Intermediates useful for the synthesis of delphinidin chloride

A process is provided for producing delphinidin which comprises reacting a compound of formula STR1 wherein each Pg represents a hydroxyl protecting group, and Lg represents a leaving group with a compound of formula STR2 wherein Pg' represents a hydroxyl protecting group characterized in that the compound of formula VII is produced from an intermediate of formula STR3 wherein each Pg" represents a hydroxyl protecting group and each Alk represents lower alkyl, by (i) subjecting the intermediate of formula IX to hydrolysis and decarboxylation to form 3,4,5-trihydroxyacetophenone of formula STR4 (ii) converting the 3,4,5-trihydroxyacetophenone to the compound of formula VII by introduction of the protecting groups Pg" and converting the group of formula --COCH3 to a group of formula --COCH2 Lg.