1353568-59-8

Basic information

• Product Name: C₁₇H₁₉IO₅
• Synonyms: C₁₇H₁₉IO₅
• CAS NO: 1353568-59-8
• Molecular Weight: 430.239
• Mol File: 1353568-59-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₇H₁₉IO₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₁₉IO₅(1353568-59-8)
• EPA Substance Registry System: C₁₇H₁₉IO₅(1353568-59-8)

Safety Data

• Hazardous Substances Data: 1353568-59-8(Hazardous Substances Data)

Upstream product

• 2314-37-6 3-iodo-4-methoxybenzaldehyde 
• 133095-91-7 3,4,5-trimethoxyphenylmagnesium bromide 

Downstream Products

• 1353568-79-2 4'-fluoro-2-methoxy-5-[1-(3,4,5-trimethoxyphenyl)vinyl]biphenyl 
• 1353568-77-0 4'-chloro-2-methoxy-5-[1-(3,4,5-trimethoxyphenyl)vinyl]biphenyl 
• 1353568-75-8 2'-methoxy-5'-[1-(3,4,5-trimethoxyphenyl)vinyl]biphenyl-4-ol 
• 1353568-72-5 2,4'-dimethoxy-5-[1-(3,4,5-trimethoxyphenyl)vinyl]biphenyl 
• 1353568-70-3 (E)-3-(2-methoxy-5-(1-(3,4,5-trimethoxyphenyl)vinyl)phenyl)-prop-2-en-1-ol 
• 1353568-68-9 (E)-3-{2-methoxy-5-[1-(3,4,5-trimethoxyphenyl)vinyl]phenyl}acrylic acid 
• 1353569-35-3 [3-(4-hydroxybut-1-ynyl)-4-methoxyphenyl](3,4,5-trimethoxyphenyl)methanone 
• 1353569-33-1 [3-(3-hydroxyprop-1-ynyl)-4-methoxyphenyl](3,4,5-trimethoxyphenyl)methanone 
• 1353569-30-8 methyl 1-(2-methoxy-5-(1-(3,4,5-trimethoxyphenyl)vinyl)phenyl)-1H-1,2,3-triazole-4-carboxylate 
• 1353569-27-3 1-{2-methoxy-5-[1-(3,4,5-trimethoxyphenyl)vinyl]phenyl}-4-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazole 
• 1353569-24-0 1-{2-methoxy-5-[1-(3,4,5-trimethoxyphenyl)vinyl]phenyl}-4-(4-methoxyphenyl)-1H-1,2,3-triazole 
• 1353569-21-7 2-azido-1-methoxy-4-[1-(3,4,5-trimethoxyphenyl)vinyl]benzene 
• 1353568-65-6 methyl (E)-3-(2-methoxy-5-(1-(3,4,5-trimethoxyphenyl)vinyl)-phenyl)acrylate 
• 1353569-19-3 4-{5-[1-(3,4,5-trimethoxyphenyl)vinyl]benzofuran-2-yl}phenol 

Relevant articles and documents

B-Ring-Modified isoCombretastatin A-4 Analogues Endowed with Interesting Anticancer Activities

A novel class of isocombretastatinA-4 (isoCA-4) analogues with modifications at the 3'-position of the B-ring by replacement with C-linked substituents was studied. Exploration of the structure-activity relationships of theses analogues led to the identif