4010-33-7

Basic information

• Product Name: O-ACETYLPHENYL BENZOATE
• Synonyms: 2-BENZOYLOXYACETOPHENONE;TIMTEC-BB SBB007859;O-ACETYLPHENYL BENZOATE;O-BENZOYLOXYACETOPHENONE;1-[2-(benzoyloxy)phenyl]-ethanon;2-Acetylphenyl benzoate;Acetophenone, 2'-hydroxy-, benzoate;Benzoic acid, 2-acetylphenyl ester
• CAS NO: 4010-33-7
• Molecular Formula: C₁₅H₁₂O₃
• Molecular Weight: 240.25
• Product Categories: Aromatic Acetophenones & Derivatives (substituted)
• Mol File: 4010-33-7.mol
• Article Data: 56

Chemical Properties

• Boiling Point: 420 °C at 760 mmHg
• Flash Point: 188.6 °C
• Appearance: /
• Density: 1.175 g/cm³
• Vapor Pressure: 2.92E-07mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: O-ACETYLPHENYL BENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: O-ACETYLPHENYL BENZOATE(4010-33-7)
• EPA Substance Registry System: O-ACETYLPHENYL BENZOATE(4010-33-7)

Safety Data

• Hazardous Substances Data: 4010-33-7(Hazardous Substances Data)

Usage

General Description

O-Acetylphenyl Benzoate is a chemical compound that is often used in various industrial applications, particularly in the production of perfumes and other aromatic compounds due to its distinct pleasant smell, which is reminiscent of various fruits and spices. The chemical formula of O-Acetylphenyl Benzoate is C15H12O3, and it is recognized for its stability and relatively low reactivity, making it suitable for numerous applications. The compound is typically in its solid form at room temperature and has a light coloration, ranging from off-white to pale yellow. It is safe to handle under standard conditions but can cause irritation if it comes into contact with the skin or eyes, or if it is ingested or inhaled.

InChI:InChI=1/C15H12O3/c1-11(16)13-9-5-6-10-14(13)18-15(17)12-7-3-2-4-8-12/h2-10H,1H3

Upstream product

• 65-85-0 benzoic acid 
• 118-93-4 o-hydroxyacetophenone 
• 100-51-6 benzyl alcohol 
• 26307-50-6 4-bromo-2-isopropyl-phenol 
• 98-88-4 benzoyl chloride 
• 582-24-1 1-phenyl-2-hydroxyethanone 
• 100-42-5 styrene 
• 108-95-2 phenol 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 31165-67-0 2'-benzyloxyacetophenone 
• 104-87-0 4-methyl-benzaldehyde 
• 108-88-3 toluene 
• 1603-99-2 2,3,4,5,6-pentadeuteriotoluene 

Downstream Products

• 93-58-3 benzoic acid methyl ester 
• 118-93-4 o-hydroxyacetophenone 
• 525-82-6 FLAVONE 
• 1025-86-1 3-bromo-2-phenyl-chromen-4-one 
• 3740-94-1 2-bromo-1-(2-hydroxyphenyl)-3-phenylpropane-1,3-dione 
• 6005-12-5 2,3-diphenyl-4H-chromen-4-one 
• 1048823-50-2 C₂₂H₁₆O₂ 
• 1047526-35-1 C₂₂H₁₆O₃ 
• 1363396-02-4 C₂₃H₁₆O₂ 
• 1048581-79-8 3-(4-chlorophenyl)-2-phenyl-4H-chromen-4-one 
• 1017073-56-1 C₂₁H₁₃ClO₂ 
• 1363396-03-5 C₂₁H₁₃FO₂ 
• 1048750-53-3 C₂₂H₁₃F₃O₂ 
• 1363396-04-6 C₂₁H₁₃NO₄ 

Relevant articles and documents

Electrochemical Aerobic Oxidative Cleavage of (sp3)C-C(sp3)/H Bonds in Alkylarenes

An electrochemistry-promoted oxidative cleavage of (sp3)C-C(sp3)/H bonds in alkylarenes was developed. Various aryl alkanes can be smoothly converted into ketones/aldehydes under aerobic conditions using a user-friendly undivided cell setup. The features of air as oxidant, scalability, and mild conditions make them attractive in synthetic organic chemistry.

Copper-catalyzed chemoselective oxidative o-aroylation of 2-acetylphenols, alkyl salicylates and 1,3-dicarbonyl compounds using styrene derivatives

A novel copper-catalyzed chemoselective oxidative O-aroylation of 2-acetylphenols, alkyl salicylates and 1,3-dicarbonyl compounds with a wide range of styrene derivatives are described. This approach provides an efficient chemoselective preparation of phenol, alkyl salicylate and enol esters in good to excellent yields. This method represents an alternative protocol for the classical esterification reactions.

Synthesis of Spiro[benzofuran-2,2'-benzo[b]thiophene]-3,3'-diones via PIDA/CuBr-Mediated Spirocyclization

A phenyliodine(III) diacetate (PIDA)/CuBr-mediated construction of the novel 3H,3'H-spiro[benzofuran-2,2'-benzo[b]thiophene]-3,3'-dione skeleton was realized from the reaction of (Z)-3-hydroxy-1-(2-hydroxyphenyl)-3-(2-halogenphenyl)prop-2-en-1-ones with p