908-11-2

Basic information

• Product Name: 2-Propen-1-one, 1,1'-(1,4-phenylene)bis[3-phenyl-
• CAS NO: 908-11-2
• Molecular Formula: C24H18O2
• Molecular Weight: 338.406
• Mol File: 908-11-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1,1'-(1,4-phenylene)bis[3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1,1'-(1,4-phenylene)bis[3-phenyl-(908-11-2)
• EPA Substance Registry System: 2-Propen-1-one, 1,1'-(1,4-phenylene)bis[3-phenyl-(908-11-2)

Safety Data

• Hazardous Substances Data: 908-11-2(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 1009-61-6 1,4-Diacetylbenzene 
• 100-52-7 benzaldehyde 
• 623-26-7 terephthalonitrile 

Downstream Products

• 73858-29-4 1-{5-Phenyl-3-[4-(5-phenyl-1-propionyl-4,5-dihydro-1H-pyrazol-3-yl)-phenyl]-4,5-dihydro-pyrazol-1-yl}-propan-1-one 
• 73858-31-8 1-{3-[4-(1-Isobutyryl-5-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-phenyl]-5-phenyl-4,5-dihydro-pyrazol-1-yl}-2-methyl-propan-1-one 
• 96504-14-2 1-acetyl-4,5-dihydro-5-(4-(1-acetyl-4,5-dihydro-3-phenylpyrazol-5-yl)phenyl)-3-phenylpyrazole 
• 3729-35-9 1,4-bis-(5-phenyl-3-isoxazolyl)benzene 
• 6715-81-7 1,5,1',5'-tetraphenyl-1H,1'H-3,3'-p-phenylene-bis-pyrazole 
• 73858-32-9 C₃₈H₃₀N₄O₂ 
• 73858-33-0 C₃₈H₃₀N₄ 
• 73858-30-7 1-{3-[4-(1-Butyryl-5-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-phenyl]-5-phenyl-4,5-dihydro-pyrazol-1-yl}-butan-1-one 
• 73858-26-1 1,1'-bis-(4-methoxy-phenyl)-5,5'-diphenyl-4,5,4',5'-tetrahydro-1H,1'H-3,3'-p-phenylene-bis-pyrazole 
• 7267-75-6 1,5,1',5'-tetraphenyl-4,5,4',5'-tetrahydro-1H,1'H-3,3'-p-phenylene-bis-pyrazole 
• 73858-28-3 1-{3-[4-(1-Acetyl-5-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-phenyl]-5-phenyl-4,5-dihydro-pyrazol-1-yl}-ethanone 
• 130898-46-3 1,4-bis-(3-phenyl-2,3-dibromopropanoyl)benzene 
• 123825-58-1 1,4-bis(4,6-diphenylpyridin-2-yl)benzene 

Relevant articles and documents

Design and synthesis of heterocyclic compounds from 1,4-diacetylbenzene with expected antimicrobial activity

IN this present work, synthesized a novel derivatives of bis-chalcones via condensation of 1,4-diacetylbenzene with different aldehydes in basic media. The reaction of chalcone derivatives 3a,b with thioglycolic acid gave compounds 4a,b. That was reacted