259209-17-1

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3-Methoxy-2-hydroxyphenyl boronic acid is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and reactivity contribute to the development of new and effective compounds for medical and agricultural applications.
Used in Organic Synthesis:
3-Methoxy-2-hydroxyphenyl boronic acid is used as a reagent in organic synthesis for the construction of carbon-carbon bonds. Its ability to form stable organoboron compounds makes it a valuable tool in the synthesis of complex organic molecules.
Used in Suzuki-Miyaura Coupling Reactions:
3-Methoxy-2-hydroxyphenyl boronic acid is used as a coupling partner in Suzuki-Miyaura coupling reactions, a widely used method for the formation of carbon-carbon bonds in the production of fine chemicals. Its participation in these reactions allows for the creation of a diverse range of chemical products with potential applications in various industries.

Upstream product

• 90-05-1 2-methoxy-phenol 

Downstream Products

• 1605329-13-2 (S)-2-(1-((5-(2-hydroxy-3-methoxyphenyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)ethyl)-5-methyl-3-phenylpyrrolo[2,1-f][ 1,2,4]triazin-4(3H)-one 
• 1440947-69-2 N-(2-(3-hydroxy-5-methoxy-3,3a,3a¹,9a-tetrahydrophenanthro[4,5-bcd]furan-3a¹-yl)ethyl)-N,4-dimethylbenzenesulfonamide 
• 90-05-1 2-methoxy-phenol 
• 1272672-11-3 7-hydroxy-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-5-oxo-4,5-dihydro-1H-pyrrolo[3,2-b]pyridine-6-carbonitrile 
• 1272674-58-4 ethyl 3-amino-5-chloro-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-1H-pyrrole-2-carboxylate 
• 1346607-53-1 ethyl 3-amino-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-1H-pyrrole-2-carboxylate hydrochloride 
• 1346608-12-5 ethyl 5-chloro-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-3-[({[1-methyl-2-(methyloxy)-2-oxoethyl]amino}carbonyl)amino]-1H-pyrrole-2-carboxylate 
• 1346608-10-3 ethyl 5-chloro-3-{[({3-[(ethyloxy)carbonyl]phenyl}amino)carbonyl]amino}-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-1H-pyrrole-2-carboxylate 
• 1346608-07-8 ethyl 5-chloro-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-3-{[({4-methyl-3-[(methyloxy)carbonyl]phenyl}amino)carbonyl]amino}-1H-pyrrole-2-carboxylate 
• 1346607-66-6 ethyl 5-chloro-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-3-{[(phenylamino)carbonyl]amino}-1H-pyrrole-2-carboxylate 
• 1346607-63-3 ethyl 3-({[(2-fluorophenyl)amino]carbonyl}amino)-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-1H-pyrrole-2-carboxylate 
• 1346607-58-6 ethyl 5-chloro-3-[({[3-(ethyloxy)-3-oxopropyl]amino}carbonyl)amino]-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-1H-pyrrole-2-carboxylate 
• 1346607-52-0 2-{6-chloro-5-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-2,4-dioxo-1,2,4,5-tetrahydro-3H-pyrrolo[3,2-d]pyrimidin-3-yl}propanoic acid 
• 1346607-49-5 1-methylethyl 3-{6-chloro-5-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-2,4-dioxo-1,2,4,5-tetrahydro-3H-pyrrolo[3,2-d]pyrimidin-3-yl}propanoate 

Relevant academic research and scientific papers

Preparation method of 3-methoxyl-2-hydroxyphenylboronic acid

The invention relates to a preparation method of 3-methoxyl-2-hydroxyphenylboronic acid. According to the method, a final product of 3-methoxyl-2-hydroxyphenylboronic acid is mainly obtained through three-step reaction of etherification hydroxyl protectio