85117-87-9

Basic information

• Product Name: 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate
• Synonyms: 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate;2-(Acetyloxy)-1-[3,4,5-tris(acetyloxy)phenyl]ethanone;Ethanone, 2-(acetyloxy)-1-[3,4,5-tris(acetyloxy)phenyl]-
• CAS NO: 85117-87-9
• Molecular Formula: C₁₆H₁₆O₉
• Molecular Weight: 352.29284
• EINECS: 285-637-4
• Mol File: 85117-87-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 500.6°C at 760 mmHg
• Flash Point: 221.2°C
• Appearance: /
• Density: 1.303g/cm³
• Vapor Pressure: 3.76E-10mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate(85117-87-9)
• EPA Substance Registry System: 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate(85117-87-9)

Safety Data

• Hazardous Substances Data: 85117-87-9(Hazardous Substances Data)

Usage

General Description

5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate is a complex chemical compound with a long name, commonly used as a crosslinking agent in the production of various polymers and resins. It is also known for its application in the pharmaceutical industry as a building block for the synthesis of certain drugs. 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate is a triester, meaning it contains three acetyl functional groups attached to a central benzene ring, which gives it the ability to form strong covalent bonds with other molecules. Its structure and reactivity make it a valuable component in the production of adhesives, coatings, and other industrial materials. Additionally, its unique properties make it a useful tool in research and development for creating new materials and chemical compounds.

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

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

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 articles and documents

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