5344-60-5

Basic information

• Product Name: methyl 4-oxo-2,4-diphenylbutanoate
• CAS NO: 5344-60-5
• Molecular Formula: C₁₇H₁₆O₃
• Molecular Weight: 268.3071
• Mol File: 5344-60-5.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 411.8°C at 760 mmHg
• Flash Point: 182°C
• Density: 1.139g/cm³
• Vapor Pressure: 5.45E-07mmHg at 25°C
• Refractive Index: 1.562
• CAS DataBase Reference: methyl 4-oxo-2,4-diphenylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-oxo-2,4-diphenylbutanoate(5344-60-5)
• EPA Substance Registry System: methyl 4-oxo-2,4-diphenylbutanoate(5344-60-5)

Safety Data

• Hazardous Substances Data: 5344-60-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 6268-00-4 4-oxo-2,4-diphenylbutanenitrile 
• 124-41-4 sodium methylate 
• 5369-54-0 2,4,2',4'-tetraphenyl-2H,2'H-[2,2']bifuranyl-5,5'-dione 
• 74-88-4 methyl iodide 
• 98-86-2 acetophenone 
• 15028-40-7 DL-2-phenylglycine methyl ester hydrochloride 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 5633-34-1 (benzoylmethylene)dimethylsulfurane 
• 22979-35-7 Methyl phenyldiazoacetate 
• 1285705-07-8 methyl (E)-4-phenyl-4-oxo-2-phenylbut-2-enoate 
• 492-38-6 2-phenylacrylic acid 
• 1865-29-8 2-phenyl-acrylic acid methyl ester 
• 611-73-4 Benzoylformic acid 

Downstream Products

• 75616-24-9 2,4,6-triphenyl-4,5-dihydro-2H-pyridazin-3-one 
• 2166-00-9 4,6-diphenylpyridazin-3(2H)-one 
• 2166-09-8 4,6-diphenyl-4,5-dihydropyridazin-3(2H)-one 
• 92541-01-0 1,3-diphenyl-1,4-butanodiol 
• 21034-29-7 2,4-diphenyl-γ-butyrolactone 
• 4370-96-1 4-oxo-2,4-diphenylbutanoic acid 
• 6267-06-7 3-bromo-4-oxo-2,4-diphenyl-butyric acid methyl ester 

Relevant articles and documents

Visible-Light-Promoted Polysubstituted Olefins Synthesis Involving Sulfur Ylides as Carbene Trapping Reagents

A blue-light-emitting diode (LED) promoted coupling of aryl diazoacetates with sulfur ylides is described. This protocol features mild conditions, good functional group tolerance, and broad substrate scope for both aryl diazoacetates with sulfur ylides. Under optimal reaction conditions, a wide range of trisubstituted olefins is obtained in moderate to good yield, which can be further transferred to other biologically important heterocycles after a two-step simple operation.

Benzothiazolines as radical transfer reagents: Hydroalkylation and hydroacylation of alkenes by radical generation under photoirradiation conditions

Novel radical transfer reagents under photoirradiation conditions were developed by the use of benzothiazoline derivatives. These reagents enabled both hydroalkylation and hydroacylation of alkenes under neutral conditions at ambient temperature without a