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 
• 1056888-83-5 5-benzyloxy-1-phenylpent-2-en-1-one 
• 93-58-3 benzoic acid methyl ester 
• 98-86-2 acetophenone 
• 504-64-3 carbon suboxide 
• 917-64-6 methyl magnesium iodide 
• 100-52-7 benzaldehyde 
• 98-88-4 benzoyl chloride 
• 591-51-5 phenyllithium 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 536-74-3 phenylacetylene 
• 144223-33-6 2-furoyl-1H-1,2,3-benzotriazole 

Downstream Products

• 3164-00-9 β-methoxycarbonyloxy-chalcone 
• 90145-35-0 2,2-Dibenzoylessigsaeure-methylester 
• 641-45-2 2-(α-hydroxy-benzylidene)-1,3-diphenyl-propane-1,3-dione 
• 611-73-4 Benzoylformic acid 
• 65-85-0 benzoic acid 
• 2085-31-6 2-diazo-1,3-diphenylpropane-1,3-dione 
• 643-75-4 1,3-diphenyl-propane-1,2,3-trione 
• 742-01-8 1,3,5-triphenyl-4,5-dihydro-1H-pyrazole 
• 143032-08-0 4-bromo-1,3,5-triphenyl-1H-pyrazole 
• 40697-44-7 4-nitroso-1,3,5-triphenyl-1H-pyrazole 
• 26429-75-4 1-methyl-2,3,5-triphenyl-pyrazolium; iodide 
• 59875-97-7 2-allyl-1,3-diphenyl-1,3-propanedione 
• 132994-41-3 2-(2-methylallyl)-1,3-diphenyl-1,3-propanedione 
• 120-46-7 1,3-diphenylpropanedione 

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.

Tf2O-Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β-Enaminones

Based on the Tf2O-mediated intermolecular reaction of secondary amides with enamines derived from ketones, a novel approach to β-enaminones has been developed. The reaction is widely functional group tolerant and highly chemoselective. In the presence of 4 ? molecular sieves, the method can be extended to the one-pot condensation of secondary amides with ketones for NH β-enaminones synthesis.