25743-56-0

Basic information

• Product Name: 4-acetoxypropiophenone
• Synonyms: 4-acetoxypropiophenone;1-(4-acetoxyphenyl)propan-1-one;Acetic acid 4-propionyl-phenyl ester
• CAS NO: 25743-56-0
• Molecular Formula: C₁₁H₁₂O₃
• Molecular Weight: 192.2112
• Mol File: 25743-56-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 59 °C
• Boiling Point: 305.3°Cat760mmHg
• Flash Point: 133.2°C
• Appearance: /
• Density: 1.097g/cm³
• Vapor Pressure: 0.000831mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: 4-acetoxypropiophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-acetoxypropiophenone(25743-56-0)
• EPA Substance Registry System: 4-acetoxypropiophenone(25743-56-0)

Safety Data

• Hazardous Substances Data: 25743-56-0(Hazardous Substances Data)

Usage

General Description

4-Acetoxypropiophenone is a chemical compound with the formula C11H12O3. It is a white solid that is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and fragrances. The compound is also known as p-acetoxypropiophenone, and it is a propiophenone that is substituted with an acetyloxy group at position 4. 4-Acetoxypropiophenone is commonly used in the synthesis of various organic compounds due to its reactivity and ability to undergo nucleophilic addition reactions. It is also used as a precursor for the production of other important chemicals and has potential applications in the pharmaceutical and chemical industries.

InChI:InChI=1/C11H12O3/c1-3-11(13)9-4-6-10(7-5-9)14-8(2)12/h4-7H,3H2,1-2H3

Upstream product

• 108-24-7 acetic anhydride 
• 70-70-2 4-hydroxypropiophenone 
• 61824-46-2 4-propylphenyl acetate 

Downstream Products

• 25743-57-1 1-(4-acetoxy-phenyl)-2-bromo-propan-1-one 
• 5965-06-0 trans-<4,4'-(diethylvinylen) bis (phenyl)>diacetate 
• 111296-25-4 N-[2-(4-acetoxy-phenyl)-1-methyl-2-oxo-ethyl]-phthalimide 
• 79010-16-5 1,3-Bis(2'-acetyl-4'-propionylphenoxy)-2-propanol 
• 79010-25-6 1-{3-Acetyl-4-[2-hydroxy-3-(4-hydroxy-4-phenyl-piperidin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79030-60-7 1-(3-Acetyl-4-{3-[2-(3,4-dimethoxy-phenyl)-ethylamino]-2-hydroxy-propoxy}-phenyl)-propan-1-one 
• 79010-31-4 1-(2'-Acetyl-4'-propionylphenoxy)-3-(4-hydroxy-4-phenylpiperidyl)propane 
• 79010-19-8 1-{3-Acetyl-4-[2-hydroxy-3-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-23-4 1-{3-Acetyl-4-[2-hydroxy-3-(4-phenyl-piperazin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-29-0 1-(2'-Acetyl-4'-propionylphenoxy)-3-(4-phenyl-3piperidienyl)propane 
• 79010-30-3 1-{3-Acetyl-4-[3-(4-phenyl-piperazin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-24-5 1-{3-Acetyl-4-[2-hydroxy-3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-26-7 1-(2'-Acetyl-4'-propionylphenoxy)-3-isopropylamino-2-propanol 
• 79010-28-9 N-<β-(2-Acetyl-4-propionylphenoxy)ethyl>pyrrolidine 

Relevant articles and documents

Visible-Spectrum Solar-Light-Mediated Benzylic C-H Oxygenation Using 9,10-Dibromoanthracene As an Initiator

We report a visible-light-mediated benzylic C-H oxygenation reaction. The reaction is initiated by solar light or the blue LED activation of 9,10-dibromoanthracene in a reaction with oxygen and takes place at ambient temperature and air pressure. Secondary benzylic positions are oxygenated to ketones, while tertiary benzylic carbons are oxygenated to give hydroperoxides. Notably, cumene hydroperoxide is produced in a higher yield and at milder conditions than the currently employed industrial conditions.