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 
• 536-74-3 phenylacetylene 
• 7338-94-5 1,3-diphenyl-2-propynone 
• 932-90-1 Benzaldoxime 
• 3235-02-7 p-methylbenzaldehyde oxime 
• 14683-79-5 salicylaldoxime 
• 3717-17-7 4-isopropylbenzaldehyde oxime 
• 3717-21-3 p-methoxyl benzaldoxime 
• 2929-84-2 4-dimethylaminobenzaldehyde oxime 
• 3848-36-0 4-chlorobenzaldoxime 
• 34158-72-0 2-bromobenzaldehyde oxime 
• 66046-34-2 4-(trifluoromethyl)benzaldehyde oxime 
• 1129-37-9 4-nitrobenzaldehyde oxime 

Downstream Products

• 3164-00-9 β-methoxycarbonyloxy-chalcone 
• 90145-35-0 2,2-Dibenzoylessigsaeure-methylester 
• 101936-34-9 (2-benzoyl-3-oxo-3-phenyl-propyl)-malononitrile 
• 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 
• 93-91-4 1-phenylbutan-1,3-dione 
• 612-96-4 2-Phenylquinoline 
• 113059-25-9 (phenyl)(2-phenylquinolin-3-yl)methanone 
• 13182-64-4 2-Isopropyl-3H-quinazolin-4-one 
• 1145-01-3 3,5-Diphenylpyrazole 
• 2039-49-8 3,5-diphehylisoxazole 
• 14097-24-6 1,3-diphenylpropan-1-ol 

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.

Enolization rates control mono-: Versus di-fluorination of 1,3-dicarbonyl derivatives

Fluorine-containing 1,3-dicarbonyl derivatives are essential building blocks for drug discovery and manufacture. To understand the factors that determine selectivity between mono- and di-fluorination of 1,3-dicarbonyl systems, we have performed kinetic studies of keto-enol tautomerism and fluorination processes. Photoketonization of 1,3-diaryl-1,3-dicarbonyl derivatives and their 2-fluoro analogues is coupled with relaxation kinetics to determine enolization rates. Reaction additives such as water accelerate enolization processes, especially of 2-fluoro-1,3-dicarbonyl systems. Kinetic studies of enol fluorination with Selectfluor and NFSI reveal the quantitative effects of 2-fluorination upon enol nucleophilicity towards reagents of markedly different electrophilicity. Our findings have important implications for the synthesis of α,α-difluoroketonic compounds, providing valuable quantitative information to aid in the design of fluorination and difluorination reactions.