72758-69-1

Basic information

• Product Name: (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one
• CAS NO: 72758-69-1
• Molecular Weight: 287.156
• Mol File: 72758-69-1.mol
• Article Data: 75

Chemical Properties

• CAS DataBase Reference: (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one(72758-69-1)
• EPA Substance Registry System: (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one(72758-69-1)

Safety Data

• Hazardous Substances Data: 72758-69-1(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 66107-30-0 4-bromophenyl trifluoromethanesulfonate 
• 66680-87-3 (E)-1-phenyl-(2-tributylstannyl)ethene 
• 100-52-7 benzaldehyde 
• 99-73-0 para-bromophenacyl bromide 
• 100-42-5 styrene 
• 589-87-7 1,4-bromoiodobenzene 
• 10342-83-3 4'-Bromopropiophenone 
• 98-80-6 phenylboronic acid 
• 1669-51-8 1‐(4‐bromophenyl)‐3‐phenylpropan‐1‐one 
• 109240-30-4 1-(4-bromophenyl)cyclopropan-1-ol 
• 1122-91-4 4-bromo-benzaldehyde 
• 536-74-3 phenylacetylene 
• 99-90-1 para-bromoacetophenone 

Downstream Products

• 134045-58-2 5-(4-Bromo-phenyl)-7-phenyl-3-phenylazo-pyrazolo[1,5-a]pyrimidin-2-ylamine 
• 102752-32-9 diethyl 2-(3-(4-bromophenyl)-3-oxo-1-phenylpropyl)malonate 
• 74918-94-8 2,6‐bis(4‐bromophenyl)‐4‐phenylpyridine 
• 133131-51-8 4-(4-bromophenyl)-4-oxo-2-phenylbutanenitrile 
• 1019637-07-0 4-(4-bromophenyl)-2-[3-(4-bromophenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl]-6-phenylpyrimidine 
• 1040232-85-6 (S)-2-[3-(4-bromophenyl)-3-oxo-1-phenylpropyl]malononitrile 
• 94360-06-2 2-[3-(4-Bromo-phenyl)-3-oxo-1-phenyl-propyl]-malononitrile 
• 1224869-07-1 (S)-1-(4-bromophenyl)-3-(diphenylphosphinyl)-3-phenylpropan-1-one 
• 1262588-25-9 C₂₇H₂₂BrO₂P 

Relevant articles and documents

Green method for high-selectivity synthesis of chalcone compounds

Under the condition of air, the water-soluble inorganic weak base is used as a catalyst to catalyze the hydrogen transfer reaction of the propargyl alcohol compound, so that the green synthesis of the high-trans selective chalcone compound is realized. Reaction temperature: 80 - 120 °C and reaction time 12 - 48 hours. To the technical scheme, any transition metal catalyst and ligand do not need to be used, inert gas protection is not needed, no other byproducts are generated, the atom economy 100%, green and environment friendliness are avoided, and the product is a high-selectivity (E)-type product. The reaction conditions are relatively low in requirement. Compared with the prior art, the alkali catalyst is obvious in advantages, and has a certain application prospect in the fields of organic synthesis, biochemistry, medicine and the like.

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Pyridoimidazole derivatives as well as preparation method and application thereof

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