4-Methoxyphenylboronic acid

• Catalog No.: 417599
• CAS Number: 5720-07-0
• M. F.: C7H9BO3
• M. W.: 151.95556
• Purity: ≥95.0%

SYNONYMS

• Title: 4-甲氧基苯硼酸
• IUPAC name: (4-methoxyphenyl)boronic acid
• IUPAC Traditional name: 4-methoxyphenylboronic acid
• Synonyms: 4-Anisylboronic acid; p-Methoxybenzeneboronic acid; (4-Methoxyphenyl)boric acid; 4-Methoxybenzeneboronic acid; (p-Methoxyphenyl)boronic acid; p-Anisylboronic acid; 对甲氧基苯硼酸

DATABASE IDS

• Beilstein Number: 2936912
• MDL Number: MFCD00039139
• CAS Number: 5720-07-0
• PubChem SID: 24866163

PROPERTIES

• Linear Formula: CH3OC6H4B(OH)2
• Purity: ≥95.0%
• Melting Point: 204-206 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• RTECS: CY8975000
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Other Notes
Contains varying amounts of anhydride
Packaging
1, 5, 25 g in glass bottle
Application
Reagent used for
• Suzuki-Miyaura cross-coupling reactions1
• Pd-catalyzed direct arylation2
• Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water3
• Palladium-catalyzed stereoselective Heck-type reaction4
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence5
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides6
• Ruthenium catalyzed direct arylation7
• Rh-catalyzed asymmetric conjugate addition8
• Ligand-free copper-catalyzed coupling9 Reagent used in Preparation of
• Palladium(II) thiocarboxamide complexes as Suzuki coupling catalyst10
• Push-pull arylvinyldiazine chromophores with photophysical properties11

Description (简体中文)

Other Notes
含不定量的酸酐
包装
1, 5, 25 g in glass bottle
Application
Reagent used for
• Suzuki-Miyaura cross-coupling reactions1
• Pd-catalyzed direct arylation2
• Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water3
• Palladium-catalyzed stereoselective Heck-type reaction4
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence5
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides6
• Ruthenium catalyzed direct arylation7
• Rh-catalyzed asymmetric conjugate addition8
• Ligand-free copper-catalyzed coupling9 Reagent used in Preparation of
• Palladium(II) thiocarboxamide complexes as Suzuki coupling catalyst10
• Push-pull arylvinyldiazine chromophores with photophysical properties11