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

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

Uses

Used in Chemical Industry:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a UV-curing agent for [application reason] its ability to facilitate the curing process of various products, enhancing their production efficiency and quality.
Used in Pharmaceutical Industry:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a raw material for [application reason] its role in the synthesis of various pharmaceuticals, contributing to the development of new drugs and treatments.
Used in Dye Production:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a starting material for [application reason] its involvement in the production of different types of dyes, which are essential for coloring fabrics, plastics, and other materials.
Used in Organic Synthesis:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a versatile building block for [application reason] its reactivity in creating a wide range of organic compounds, which can be applied in various fields, including materials science and specialty chemicals.
Used in UV-curable Coatings and Inks:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a photoinitiator for [application reason] its capacity to initiate the curing process of UV-curable coatings and inks, leading to faster drying times and improved product performance.

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 
• 1776-30-3 (E)-2',4'-dihydroxychalcone 
• 6665-86-7 7-hydroxyflavone 
• 38214-70-9 4-(5-Phenyl-1H-pyrazol-3-yl)-benzene-1,3-diol 
• 132454-22-9 Benzoic acid 3-hydroxy-4-(5-phenyl-isoxazol-3-yl)-phenyl ester 
• 132454-21-8 Benzoic acid 4-(1,5-diphenyl-1H-pyrazol-3-yl)-3-hydroxy-phenyl ester 
• 38256-07-4 1-(2',4'-dihydroxyphenyl)-3-phenyl-propane-1,3-dione 
• 961-29-5 isoliquirtigenin 
• 1345025-30-0 C₂₉H₂₀O₆ 
• 109817-89-2 7-dichloroacetoxy-2-phenyl-chromen-4-one 
• 3168-24-9 7-chloroacetoxy-2-phenyl-chromen-4-one 
• 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

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This research communication is toward the investigation of the antibacterial, antifungal and antioxidant activities of the synthesized compounds 1-(4′-O-β-d-glucopyranosyloxy-2′-hydroxyphenyl)-3- aryl-propane-1,3-diones (5a)-(5h). These compounds have bee

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