29816-74-8

Basic information

• Product Name: 2-Propen-1-one, 3-(3-bromophenyl)-1-phenyl-
• CAS NO: 29816-74-8
• Molecular Formula: C15H11BrO
• Molecular Weight: 287.156
• Mol File: 29816-74-8.mol
• Article Data: 40

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 3-(3-bromophenyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 3-(3-bromophenyl)-1-phenyl-(29816-74-8)
• EPA Substance Registry System: 2-Propen-1-one, 3-(3-bromophenyl)-1-phenyl-(29816-74-8)

Safety Data

• Hazardous Substances Data: 29816-74-8(Hazardous Substances Data)

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 98-86-2 acetophenone 
• 70-11-1 α-bromoacetophenone 
• 5399-30-4 2-oxo-2-phenylethylthiocyanate 
• 15852-73-0 (3-Bromophenyl)methanol 
• 536-74-3 phenylacetylene 
• 89598-96-9 (3-bromophenyl)boronic acid 
• 93-55-0 1-phenyl-propan-1-one 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 603-33-8 triphenylbismuthane 
• 59114-87-3 (E)-3-(3-bromophenyl)-N,N-diethylacrylamide 

Downstream Products

• 80824-89-1 2-[1-(3-Bromo-phenyl)-3-oxo-3-phenyl-propylsulfanyl]-benzoic acid 
• 606-86-0 1,3,3-triphenylpropan-1-one 
• 1006876-77-2 4-(3-bromophenyl)-6-phenyl-(1H)-pyrimidin-2-one 
• 67005-18-9 6-(3-Bromo-phenyl)-4-phenyl-1H-pyrimidine-2-thione 
• 77153-42-5 (cis)-1-(m-Bromophenyl)-2-phenylcyclopropane 
• 77153-43-6 (trans)-1-(m-Bromophenyl)-2-phenylcyclopropane 
• 65565-12-0 3-(3-bromophenyl)-1-phenyl-propan-1-one 
• 1196864-46-6 4-(3-bromophenyl)-2-phenyl-4,5-dihydro-3H-pyrido[2,3-b][1,4]diazepine 
• 1196864-47-7 8-bromo-4-(3-bromophenyl)-2-phenyl-4,5-dihydro-3H-pyrido[2,3-b][1,4]diazepine 
• 77738-96-6 2-(3-bromo-phenyl)-1H-benzoimidazole 
• 346685-14-1 2-(3-bromophenyl)-4-phenyl-2,3-dihydro-1H-benzo[b][1,4]diazepine 
• 1196864-42-2 7,8-dibromo-2-(3-bromophenyl)-4-phenyl-2,3-dihydro-1H-benzo[b][1,4]diazepine 
• 1236384-44-3 N-(3-benzyl-4-(3-bromophenyl)-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-yl)benzamide 
• 1337883-33-6 3-(3-bromophenyl)-1,5-diphenyl-2-pyrazoline 

Relevant articles and documents

Rapid umpolung Michael addition of isatin N, N ′-cyclic azomethine imine 1,3-dipoles with chalcones

The umpolung Michael addition of isatin N,N′-cyclic azomethine imine 1,3-dipoles with chalcones is reported. The reaction could be finished within a very short time (0.3-2 min), with 3,3-disubstituted oxindole derivatives obtained in moderate to excellent yields with promising dr values. Unusual Michael adducts were obtained in moderate to high yields (26-98%) with low to high diastereoselectivities (0.8: 1 to 8.5: 1 dr). All the synthesized compounds (3, 3′, 4, 5, 5′, 7, 7′, 9 and 9′) were well characterized by FTIR, NMR, and mass spectral analyses and further confirmed by the single-crystal X-ray diffraction analysis of compounds 3aa and 4n.

Novel indolo[3,2,1-jk]carbazole-based bipolar host material for highly efficient thermally activated delayed-fluorescence organic light-emitting diodes

A novel bipolar material (ICzPyr) composed of electron-donating indolo[3,2,1-jk]carbazole and electron-withdrawing pyridmidine was developed and its use as a host material in thermally activated delayed-fluorescence (TADF) organic light-emitting diode (OL

N-Heterocyclic Carbene Catalyzed Synthesis of Trisubstituted Epoxides via Tandem Amidation/Epoxidation Sequence

A tandem amidation/epoxidation sequence between various substituted chalcones and N,N-dimethylformamide (DMF) for the synthesis of trisubstituted epoxides employing N-heterocyclic carbene catalysis was developed. This reaction was performed under metal-free conditions in the presence of tert-butyl hydroperoxide (TBHP) as the oxidant. Trisubstituted epoxides bearing a ketone and an amide functionality (N,N-dimethyl formyl group) were synthesized starting from a wide range of chalcones in moderate to good yields with excellent diastereoselectivity.