66832-97-1

Basic information

• Product Name: 1-(2,4-Bis(benzoyloxy)phenyl)ethanone
• Synonyms: 1-(2,4-Bis(benzoyloxy)phenyl)ethanone;2,4-Di(benzoyloxy)acetophenone;2,4-Dihydroxyacetophenonedibenzoate;4-acetyl-1,3-phenylene dibenzoate
• CAS NO: 66832-97-1
• Molecular Formula: C₂₂H₁₆O₅
• Molecular Weight: 360.36
• Mol File: 66832-97-1.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(2,4-Bis(benzoyloxy)phenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-Bis(benzoyloxy)phenyl)ethanone(66832-97-1)
• EPA Substance Registry System: 1-(2,4-Bis(benzoyloxy)phenyl)ethanone(66832-97-1)

Safety Data

• Hazardous Substances Data: 66832-97-1(Hazardous Substances Data)

Usage

General Description

1-(2,4-Bis(benzoyloxy)phenyl)ethanone is an organic compound with the chemical formula C28H20O5. It is a white crystalline solid that is commonly used as a UV-curing agent and as a raw material in the production of pharmaceuticals and dyes. The compound has two benzoyloxy groups attached to a phenyl ring, which is in turn connected to an ethanone group. It is widely used in the production of various products in the chemical and pharmaceutical industries, due to its reactivity and versatility. Additionally, 1-(2,4-Bis(benzoyloxy)phenyl)ethanone has applications in the field of organic synthesis and as a photoinitiator for UV-curable coatings and inks.

Upstream product

• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 98-88-4 benzoyl chloride 
• 65-85-0 benzoic acid 

Downstream Products

• 5465-06-5 <4-(benzoyloxy)-2-hydroxybenzoyl>benzoylmethane 
• 117096-61-4 7-hydroxy-2-phenyl-3-benzoylchromone 
• 258856-60-9 2',4'-dibenzoyloxy-2-bromoacetophenone 
• 38256-07-4 1-(2',4'-dihydroxyphenyl)-3-phenyl-propane-1,3-dione 
• 1345025-30-0 C₂₉H₂₀O₆ 
• 961-29-5 isoliquirtigenin 
• 109817-89-2 7-dichloroacetoxy-2-phenyl-chromen-4-one 
• 3168-24-9 7-chloroacetoxy-2-phenyl-chromen-4-one 
• 132454-21-8 Benzoic acid 4-(1,5-diphenyl-1H-pyrazol-3-yl)-3-hydroxy-phenyl ester 
• 132454-22-9 Benzoic acid 3-hydroxy-4-(5-phenyl-isoxazol-3-yl)-phenyl ester 
• 38214-70-9 4-(5-Phenyl-1H-pyrazol-3-yl)-benzene-1,3-diol 
• 107127-91-3 [2-(2,4-Bis-benzoyloxy-phenyl)-2-oxo-ethyl]-triphenyl-phosphonium; bromide 
• 107127-92-4 1-(2,4-Dihydroxy-phenyl)-2-(triphenyl-λ⁵-phosphanylidene)-ethanone 
• 107127-94-6 7-Hydroxy-2-(2-nitro-phenyl)-chromen-4-one 

Relevant articles and documents

One-pot synthesis of 3-fluoroflavones: Via 1-(2-hydroxyphenyl)-3-phenylpropane-1,3-diones and selectfluor at room temperature

A concise and efficient one-pot strategy to synthesize 3-fluoroflavones was developed. 1-(2-Hydroxyphenyl)-3-phenylpropane-1,3-diones were fluorinated using selectfluor with a small amount of CH3CN at room temperature, followed by cyclization a

Crystal structure and luminescence properties of 4-(4-benzoyloxy-2- hydroxyphenyl)-2,2-difluoro-6-phenyl-1,3,2-dioxaborine

The crystal structure of 4-(4-benzoyloxy-2-hydroxyphenyl)-2,2- difluoro6phenyl-1,3,2-dioxaborine (1) was determined by X-ray diffraction analysis. π-π-Stacking interaction between the molecules results in joining the molecules into a threedimensional laye

Reinvestigation of the synthesis of isoliquiritigenin: Application of Horner-Wadsworth-Emmons reaction and Claisen-Schmidt condensation

Isoliquiritigenin [ILG, (E)-1] was readily prepared via the Horner-Wadsworth-Emmons reactions using β -ketophosphonates 5a, b. An improved protocol for the synthesis of (E)-1 via the Claisen-Schmidt condensation was also presented.