62961-62-0

Basic information

• Product Name: 2-Propen-1-one, 3-hydroxy-1,3-diphenyl-, (Z)-
• CAS NO: 62961-62-0
• Molecular Formula: C15H12O2
• Molecular Weight: 224.259
• Mol File: 62961-62-0.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 3-hydroxy-1,3-diphenyl-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 3-hydroxy-1,3-diphenyl-, (Z)-(62961-62-0)
• EPA Substance Registry System: 2-Propen-1-one, 3-hydroxy-1,3-diphenyl-, (Z)-(62961-62-0)

Safety Data

• Hazardous Substances Data: 62961-62-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 5411-12-1 chalcone epoxide 
• 7570-85-6 trans-2,3-epoxy-1,3-diphenyl-1-propanone 
• 93-58-3 benzoic acid methyl ester 
• 98-86-2 acetophenone 
• 120-46-7 1,3-diphenylpropanedione 
• 504-64-3 carbon suboxide 
• 1907-69-3 3-ethoxy-1,3-diphenylprop-2-en-1-one 
• 838-58-4 1-phenylvinyl benzoate 
• 611-91-6 trans-2,3-dibromo-1,3-diphenylpropan-1-one 
• 1907-69-3 (Z)-3-ethoxy-1,3-diphenylprop-2-en-1-one 
• 93321-59-6 4-Benzoyl-3-phenylbut-2-enoic acid 
• 917-64-6 methyl magnesium iodide 
• 100-52-7 benzaldehyde 

Downstream Products

• 3164-00-9 β-methoxycarbonyloxy-chalcone 
• 90145-35-0 2,2-Dibenzoylessigsaeure-methylester 
• 1145-01-3 3,5-Diphenylpyrazole 
• 16232-42-1 3-cyano-4,6-diphenyl-2-pyridone 
• 849-01-4 1,3,3-triphenylprop-2-en-1-one 
• 6624-02-8 3-hydroxy-1,3,3-triphenyl-propan-1-one 
• 93-89-0 benzoic acid ethyl ester 
• 98-86-2 acetophenone 
• 40230-24-8 2-amino-4,6-diphenylpyrimidine 
• 19221-93-3 2-acetyldibenzoylmethane 
• 93-91-4 1-phenylbutan-1,3-dione 
• 728-84-7 2-bromo-1,3-diphenylpropane-1,3-dione 
• 13182-64-4 2-Isopropyl-3H-quinazolin-4-one 
• 2039-49-8 3,5-diphehylisoxazole 

Relevant articles and documents

Diverse One-Pot Electrophilic Trapping Reactions of 2-Quinolyl zincates with Acyl Chlorides and Allyl Iodide

The tandem acylation reactions of 2-quinolylzincates under one-pot reaction conditions facilitated the formation of biologically active (Z)-3-alkylidenephthalides and multifunctionalized quinoline derivatives at specific positions. The reactions of these

Synthesis of Perinaphthenones via BF3.Et2O Mediated One-Pot Cascade 4,5-Annulation Reactions of 1-Naphthols and Ynones

C4-C5 periannulation of 1-naphthols and ynones via BF3.Et2O mediated one-pot cascade under metal and solvent-free conditions have been developed for the synthesis of perinaphthenones. Furthermore, thi

Metal complex and electroluminescent device comprising same

Disclosed are a metal complex and an electroluminescent device comprising the same, wherein the metal complex contains a novel structure composed of a metal and a ligand. According to the invention, when the metal complex is applied to an electroluminescent device, especially in a hole injection layer, a hole transport layer and the like, the luminescent performance of the device can be improved,and the service life of the device can be effectively prolonged.

Synthesis of α,β-alkynyl ketones via the nickel catalysed carbonylative Sonogashira reaction using oxalic acid as a sustainable C1 source

An efficient and economic nickel-dppb catalyzed, carbonylative Sonogashira cross-coupling reaction was demonstrated to provide rapid access to various α,β-alkynyl ketones from aryl iodides and terminal alkynes using oxalic acid as the ex situ C1 source in a double vial (DV) system. Notably, the role of the ligand in combination with the Ni catalyst for the selective formation of carbonylative Sonogashira products was investigated and supported with control experiments. Yet, no reports are available for carbonylative Sonogashira coupling by using a CO-surrogate under Ni-catalyzed conditions. In this process, for the first time, oxalic acid is used as an ex situ solid, bench stable, easy to handle and efficient CO surrogate in a DV-system for the carbonylative Sonogashira coupling reaction with vast substrate scope.