516465-82-0

Usage

Uses

Used in Pharmaceutical Industry:
3-Isopropoxy-4-methoxyphenylboronic acid is used as a key intermediate for the synthesis of complex organic compounds, particularly in the development of new drugs. Its unique reactivity and bonding properties, due to the presence of methoxy and isopropoxy groups, make it a valuable component in the Suzuki coupling reaction, a fundamental process in the creation of pharmaceutical compounds.
Used in Agrochemical Industry:
3-Isopropoxy-4-methoxyphenylboronic acid is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its involvement in the Suzuki coupling reaction allows for the formation of complex organic molecules that can be tailored to target specific pests or weeds, improving the effectiveness and selectivity of these agrochemicals.
Used in Chemical Research:
3-Isopropoxy-4-methoxyphenylboronic acid is used as a research tool for studying the properties and reactions of organoboronic acids. Its unique structure and reactivity make it an interesting subject for chemists to explore, potentially leading to new insights and applications in various fields of chemistry.

Upstream product

• 90-05-1 2-methoxy-phenol 
• 37942-01-1 5-bromo-2-methoxyphenol 
• 98910-57-7 2-methoxyphenyl mesylate 
• 21702-84-1 2,4-dibromoanisole 
• 871571-19-6 5-bromo-2-methoxyphenyl methanesulfonate 
• 462092-23-5 4-bromo-2-isopropoxy-1-methoxybenzene 

Downstream Products

• 875654-40-3 dimethyl 3-(3-isopropoxy-4-methoxyphenyl)-1-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-4-(trifluoromethanesulfonyloxy)pyrrole-2,5-dicarboxylate 
• 895632-68-5 1-[2-(3,4-dimethoxy-phenyl)-ethyl]-3-(3-isopropoxy-4-methoxy-phenyl)-4-trifluoromethanesulfonyloxy-1H-pyrrole-2,5-dicarboxylic acid dimethyl ester 
• 1519002-15-3 methyl 4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1519002-20-0 methyl 4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-3-(3,4,5-trimethoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1519002-19-7 methyl 3-(3,4-dimethoxyphenyl)-4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1519002-18-6 methyl 4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-3-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1519002-17-5 methyl 4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-3-phenyl-1H-pyrrole-2-carboxylate 
• 1519002-16-4 methyl 3-bromo-4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1519002-27-7 3-(2,2-dimethoxyethyl)-7-isopropoxy-1-(3-isopropoxy-4-methoxyphenyl)-2-(4-isopropoxy-3-methoxyphenyl)-8-methoxy[1]benzopyrano[3,4-b]pyrrol-4(3H)-one 
• 1519002-26-6 3,11-diisopropoxy-14-(3-isopropoxy-4-methoxyphenyl)-2,12-dimethoxy-9-(phenylsulfanyl)-8,9-dihydro-6H-[1]-benzopyrano[4′,3′:4,5]pyrrolo[2,1-a]isoquinolin-6-one 
• 1519002-24-4 7-isopropoxy-1-(3-isopropoxy-4-methoxyphenyl)-2-(4-isopropoxy-3-methoxyphenyl)-8-methoxy-3-[2-(phenylsulfanyl)ethyl][1]benzopyrano[3,4-b]pyrrol-4(3H)-one 
• 1519002-23-3 7-isopropoxy-1-(3-isopropoxy-4-methoxyphenyl)-2-(4-isopropoxy-3-methoxyphenyl)-8-methoxy-[1]benzopyrano[3,4-b]pyrrol-4(3H)-one 
• 1519002-22-2 methyl 4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-5-methoxy-2-methoxymethoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1519002-21-1 methyl 3-(4,5-dimethoxy-2-methoxymethoxyphenyl)-4-(3-isopropoxy-4-methoxyphenyl)-5-(4-isopropoxy-3-methoxyphenyl)-1H-pyrrole-2-carboxylate 

Relevant academic research and scientific papers

Total synthesis of lamellarins D, L, and N

Total synthesis of cytotoxic marine alkaloids, lamellarins D, L, and N, has been achieved by using Hinsberg-type pyrrole synthesis and palladium-catalyzed Suzuki-Miyaura coupling of the 3,4-dihydroxypyrrole bistriflate 6 as the key reactions. The total yields of lamellarins D, L, and N from the common intermediate 6 are 54, 58, and 50%, respectively.