22966-09-2

Basic information

• Product Name: (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one
• Synonyms: (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one;(E)-β-(4-Bromophenyl)acrylophenone;(E)-3-(4-BROMOPHENYL)-1-PHENYLPROP-2-EN-1-ONE
• CAS NO: 22966-09-2
• Molecular Formula: C₁₅H₁₁BrO
• Molecular Weight: 287.1512
• Mol File: 22966-09-2.mol
• Article Data: 91

Chemical Properties

• Boiling Point: 398.3°Cat760mmHg
• Flash Point: 79.6°C
• Appearance: /
• Density: 1.393g/cm³
• Vapor Pressure: 1.49E-06mmHg at 25°C
• Refractive Index: 1.646
• CAS DataBase Reference: (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one(22966-09-2)
• EPA Substance Registry System: (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one(22966-09-2)

Safety Data

• Hazardous Substances Data: 22966-09-2(Hazardous Substances Data)

Usage

General Description

(E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one, also known as chalcone, is a chemical compound with the molecular formula C15H11BrO. It is a yellow crystalline solid that is commonly used in the synthesis of various other organic compounds. Chalcones, including (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one, have been widely studied for their potential pharmacological properties, such as antioxidant, anti-inflammatory, and anticancer activities. Additionally, chalcones have been investigated for their potential applications in food preservatives and dyes. Overall, (E)-1-Phenyl-3-(4-bromophenyl)-2-propene-1-one is a versatile compound with various potential uses in the fields of chemistry, pharmacology, and materials science.

InChI:InChI=1/C15H11BrO/c16-14-9-6-12(7-10-14)8-11-15(17)13-4-2-1-3-5-13/h1-11H/b11-8+

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
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• 70-11-1 α-bromoacetophenone 
• 73654-15-6 (Z)-3-(4-Bromo-phenyl)-1-phenyl-propenone 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 10388-32-6 1-phenyl-3-(4-bromophenyl)-2,3-dibromo-1-propanone 
• 96-09-3 styrene oxide 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 536-74-3 phenylacetylene 
• 135885-91-5 3-Benzoyl-2,6-bis-(4-bromo-phenyl)-1-cyano-4-hydroxy-4-phenyl-cyclohexanecarboxylic acid ethyl ester 
• 1200-07-3 trans-4-bromocinnamic acid 
• 71-43-2 benzene 
• 57-13-6 urea 

Downstream Products

• 89451-26-3 4-(4-Bromo-phenyl)-6-hydroxy-6-phenyl-2-thioxo-piperidine-3-carbonitrile; compound with piperidine 
• 101855-03-2 3-(4-bromo-phenyl)-3-methoxyamino-1-phenyl-propan-1-one 
• 107710-41-8 Dithiocarbamic acid 1-(4-bromo-phenyl)-3-oxo-3-phenyl-propyl ester 
• 27730-00-3 rac-((2R,3S)-3-(4-bromophenyl)oxiran-2-yl)(phenyl)methanone 
• 1027245-31-3 4-[1-(4-Bromo-phenyl)-3-oxo-3-phenyl-propyl]-3,4-dihydro-1H-benzo[b]azepine-2,5-dione 
• 606-86-0 1,3,3-triphenylpropan-1-one 
• 330961-77-8 (2R,3R)-3-(4-Bromo-phenyl)-2-methyl-1,5-diphenyl-pentane-1,5-dione 
• 77472-76-5 (3-(4-bromophenyl)aziridin-2-yl)(phenyl)methanone 
• 5472-01-5 3-(4-bromophenyl)-1,3-diphenylpropan-1-one 
• 219607-51-9 3-(4-bromophenyl)-4-nitro-1-phenylbutan-1-one 

Relevant articles and documents

Continuous-Flow Synthesis of Pyrylium Tetrafluoroborates: Application to Synthesis of Katritzky Salts and Photoinduced Cationic RAFT Polymerization

Katritzky salts have emerged as effective alkyl radical sources upon metal- or photocatalysis. These are typically prepared from the corresponding triarylpyrylium ions, in turn an important class of photocatalysts for small molecules synthesis and photopolymerization. Here, a flow method for the rapid synthesis of both pyrylium and Katrizky salts in a telescoped fashion is reported. Moreover, several pyrylium salts were tested in the photoinduced RAFT polymerization of vinyl ethers under flow and batch conditions.

Synthesis, crystal structure, Hirshfeld surface analysis and DNA binding studies of 1-((E)-3-(4-bromophenyl)-1-phenylallylidene)-2-(m-tolyl)hydrazine

1-((E)-3-(4-bromophenyl) -1-phenylallylidene)-2-(m-tolyl)hydrazine (4) was synthesized and characterized for structural elucidation by spectroscopy (FT-IR, 1H NMR, and 13C NMR) and single crystal X-ray diffraction. In the title compo

Deep blue fluorescent material with a narrow FWHM based on indolo[3,2,1-jk]carbazol/pyrimidine hybrids

A series of blue fluorescent materials containing electron accepting pyrimidine and electron donating bis(biphenyl)amine, diphenylcarbazole, and diphenylindolo[3,2,1-jk]carbazole moieties were synthesized in moderate yields, and their optical and electroc

Chemoselective reduction of ?,￠-unsaturated carbonyl and carboxylic compounds by hydrogen iodide

The selective reduction of ?,￠-unsaturated carbonyl compounds was achieved to produce saturated carbonyl compounds with aqueous HI solution. The introduction of an aryl group at an ? or ￠ position efficiently facilitated the reduction with good yield. The reaction was applicable to compounds bearing carboxylic acids and halogen atoms. Through the investigation of the reaction mechanism, it was found that Michael-type addition of iodide occurred to produce ￠-iodo compounds followed by the reduction of C-I bond via anionic and radical paths.