91671-15-7

Basic information

• Product Name: methyl 3-(4-acetylphenyl)propanoate
• Synonyms: methyl 3-(4-acetylphenyl)propanoate
• CAS NO: 91671-15-7
• Molecular Formula: C₁₂H₁₄O₃
• Molecular Weight: 0
• Mol File: 91671-15-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 317.6°Cat760mmHg
• Flash Point: 138.5°C
• Appearance: /
• Density: 1.083g/cm³
• Vapor Pressure: 0.000381mmHg at 25°C
• Refractive Index: 1.509
• CAS DataBase Reference: methyl 3-(4-acetylphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(4-acetylphenyl)propanoate(91671-15-7)
• EPA Substance Registry System: methyl 3-(4-acetylphenyl)propanoate(91671-15-7)

Safety Data

• Hazardous Substances Data: 91671-15-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14O3/c1-9(13)11-6-3-10(4-7-11)5-8-12(14)15-2/h3-4,6-7H,5,8H2,1-2H3

Upstream product

• 186581-53-3 diazomethane 
• 39105-51-6 3-(4-acetylphenyl)propionic acid 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 75-36-5 acetyl chloride 
• 13329-40-3 4-Iodoacetophenone 
• 158613-23-1 methyl 3-(trifluorosilyl)propanoate 
• 99-90-1 para-bromoacetophenone 
• 99-91-2 para-chloroacetophenone 
• 292638-85-8 acrylic acid methyl ester 
• 2021-28-5 ethyl dihydrocinnamate 
• 6337-70-8 3-(4-(methylcarbonyl)phenyl)propanoic acid ethyl ester 
• 3395-91-3 Methyl 3-bromopropionate 
• 501-52-0 3-Phenylpropionic acid 
• 109613-00-5 4-acetophenyl triflate 

Downstream Products

• 5467-32-3 3-(4-bromoacetyl-phenyl)-propionic acid methyl ester 
• 39105-51-6 3-(4-acetylphenyl)propionic acid 
• 5472-63-9 3-(4-azidoacetyl-phenyl)-propionic acid methyl ester 
• 5472-64-0 3-[4-(N,N-phthaloyl-glycyl)-phenyl]-propionic acid methyl ester 
• 1361413-45-7 3-(4-{[2-({[4-(ethylsulfonyl)phenyl]acetyl}amino)-4-phenyl-1,3-thiazol-5-yl] carbonyl}phenyl)propanoic acid 
• 1361414-42-7 methyl 3-{4-[(2-amino-4-phenyl-1,3-thiazol-5-yl)carbonyl]phenyl}propanoate 
• 54405-46-8 methyl 3-[4-(acetylamino)phenyl]propanoate 

Relevant articles and documents

A simple route to 1,4-addition reactions by Co-catalyzed reductive coupling of organic tosylates and triflates with activated alkenes

An efficient Co-catalyzed 1,4-addition reaction of alkyl/aryl triflates and tosylates with activated alkenes is described. In this reaction, an air-stable cobalt(ii) complex, a mild reducing agent Zn and a simple proton source (H2O) are used. A radical mechanism for the addition of alkyl tosylates to activated alkenes is likely involved.

Direct synthesis of ester-containing indium homoenolate and its application in palladium-catalyzed cross-coupling with aryl halide

An efficient method for the synthesis of ester-containing indium homoenolate via a direct insertion of indium into β-halo ester in the presence of CuI/LiCl was described. The synthetic utility of the indium homoenolate was demonstrated by palladium-cataly

Addition of electrochemically prepared arylzinc species onto activated olefins via a cobalt catalysis

The consumable anode process allows the electrochemical preparation of arylzinc compounds in the presence of cobalt chloride as catalyst in a mixed solvent acetonitrile/pyridine (9:1). Conjugate addition of these organometallic reagents to olefins is also obtained in good yields via a new method using CoBr2(2,2′-bipyridine)2 as catalyst.