259209-17-1

Basic information

• Product Name: 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID
• Synonyms: 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID;2-hydroxy-3-methoxyphenylboronic acid;REF DUPL: 3-Methoxy-2-hydroxyphenylboronic acid;[2-hydroxy-3-(Methyloxy)phenyl]boronic acid;Boronic acid,B-(2-hydroxy-3-methoxyphenyl)-
• CAS NO: 259209-17-1
• Molecular Formula: C₇H₉BO₄
• Molecular Weight: 167.95496
• Product Categories: Aryl;Organoborons
• Mol File: 259209-17-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 356.6±52.0 °C(Predicted)
• Appearance: /
• Density: 1.32±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 8.18±0.58(Predicted)
• CAS DataBase Reference: 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID(259209-17-1)
• EPA Substance Registry System: 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID(259209-17-1)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 259209-17-1(Hazardous Substances Data)

Usage

General Description

3-Methoxy-2-hydroxyphenyl boronic acid is a chemical compound with the molecular formula C7H9BO4. It is commonly used as a reagent in organic synthesis, particularly in the construction of carbon-carbon bonds. 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID has been found to be effective in the preparation of various pharmaceuticals and agrochemicals. Additionally, its boronic acid functional group allows it to participate in Suzuki-Miyaura coupling reactions, which are widely used in the production of fine chemicals. Overall, 3-methoxy-2-hydroxyphenyl boronic acid is a versatile and important chemical in the field of organic chemistry.

Upstream product

• 90-05-1 2-methoxy-phenol 

Downstream Products

• 1272672-25-9 2-chloro-7-hydroxy-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-5-oxo-4,5-dihydro-1H-pyrrolo[3,2-b]pyridine-6-carbonitrile 
• 1346608-16-9 5-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-3-(3-pyridinyl)-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione 
• 1346606-83-4 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}propanoic acid 
• 1346607-24-6 5-{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}-2-methylbenzoic acid 
• 1346606-89-0 6-chloro-5-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-3-phenyl-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione 
• 1346607-45-1 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}-N-methylpropanamide 
• 1346607-46-2 ethyl 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 
• 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 
• 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 
• 1346607-58-6 ethyl 5-chloro-3-[({[3-(ethyloxy)-3-oxopropyl]amino}carbonyl)amino]-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-1H-pyrrole-2-carboxylate 
• 1346607-63-3 ethyl 3-({[(2-fluorophenyl)amino]carbonyl}amino)-1-[2'-hydroxy-3'-(methyloxy)-4-biphenylyl]-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 
• 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 
• 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 

Relevant articles and documents

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