79324-79-1

Basic information

• Product Name: Ethanone, 1-(3,5-dibromo-4-methoxyphenyl)-
• CAS NO: 79324-79-1
• Molecular Formula: C9H8Br2O2
• Molecular Weight: 307.969
• Mol File: 79324-79-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(3,5-dibromo-4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3,5-dibromo-4-methoxyphenyl)-(79324-79-1)
• EPA Substance Registry System: Ethanone, 1-(3,5-dibromo-4-methoxyphenyl)-(79324-79-1)

Safety Data

• Hazardous Substances Data: 79324-79-1(Hazardous Substances Data)

Upstream product

• 77-78-1 dimethyl sulfate 
• 2887-72-1 1-(3,5-dibromo-4-hydroxyphenyl)ethan-1-one 
• 74-88-4 methyl iodide 
• 99-93-4 4-Hydroxyacetophenone 

Downstream Products

• 4073-35-2 3,5-dibromo-4-methoxybenzoic acid 
• 1007893-78-8 (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone 
• 1007893-79-9 (6-bromo-9H-pyrido[3,4-b]indol-1-yl)(3,5-dibromo-4-hydroxyphenyl)methanone 
• 1007893-80-2 (7-bromo-9H-pyrido[3,4-b]indol-1-yl)(3,5-dibromo-4-hydroxyphenyl)methanone 
• 1219101-98-0 C₁₆H₁₃Br₂NO₂ 
• 1204389-24-1 (2E)-1-(3,5-dibromo-4-methoxyphenyl)-3-(3,4-dimethoxyphenyl)-2-propen-1-one 
• 1085384-15-1 (2E)-1-(3,5-dibromo-4-methoxyphenyl)-3-phenyl-2-propen-1-one 
• 1063635-53-9 (2E)-1-(3,5-dibromo-4-methoxyphenyl)-3-(2-nitrophenyl)-2-propen-1-one 
• 1063635-48-2 (2E)-1-(3,5-dibromo-4-methoxyphenyl)-3-(4-(N,N-dimethylamino)phenyl)-2-propen-1-one 
• 1063635-59-5 C₁₆H₁₂Br₂O₃ 
• 1063635-51-7 (2E)-1-(3,5-dibromo-4-methoxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one 

Relevant articles and documents

Synthesis and antibacterial activities of cadiolides A, B and C and analogues

The one-pot multicomponent synthesis of natural butenolides named cadiolides A, B, C and analogues has been realized. The antibacterial structure activity relationship shows that the presence of phenolic hydroxyl groups and the number and position of bromine atoms on the different aromatic rings are important features for antibacterial activity, besides it was demonstrated the tolerance of both benzene and furan ring at position 3 of the butenolide nucleus. Furthermore, none of the most relevant antibacterial compounds showed any cytotoxicity in freshly isolated human neutrophils.