851335-07-4

Basic information

• Product Name: 4-Carboxy-2-fluorobenzeneboronic acid
• Synonyms: 4-Borono-3-fluorobenzoic acid;4-Carboxy-2-fluorobenzeneboronic acid;4-Carboxy-2-fluorobenzeneboronic acid 98%;4-Carboxy-2-fluorobenzeneboronicacid98%;4-Carboxy-2-fluorophenylboronic Acid (contains varying amounts of Anhydride);Benzoic acid,4-borono-3-fluoro- (9CI)
• CAS NO: 851335-07-4
• Molecular Formula: C₇H₆BFO₄
• Molecular Weight: 183.9295432
• Product Categories: blocks;BoronicAcids;Carboxes;Aryl;Organoborons
• Mol File: 851335-07-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 402.6 °C at 760 mmHg
• Flash Point: 197.3 °C
• Appearance: /
• Density: 1.49 g/cm³
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 3.74±0.10(Predicted)
• CAS DataBase Reference: 4-Carboxy-2-fluorobenzeneboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Carboxy-2-fluorobenzeneboronic acid(851335-07-4)
• EPA Substance Registry System: 4-Carboxy-2-fluorobenzeneboronic acid(851335-07-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 851335-07-4(Hazardous Substances Data)

Usage

Uses

suzuki reaction

Upstream product

• 871126-22-6 (2-fluoro-4-formylphenyl)boronic acid 

Downstream Products

• 1050423-87-4 2-(4'-carboxy-2'-fluorophenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane 
• 1092500-69-0 2-fluoro-4-(morpholine-4-carbonyl)boronic acid 
• 1464153-91-0 4-(3-(4-cyanophenyl)imidazo[1,2-a]pyrazin-6-yl)-3-fluorobenzoic acid 
• 1392809-29-8 4-(1-(3,5-dimethylphenylsulfonyl)-1H-indazol-3-yl)-3-fluorobenzoic acid 
• 1383379-67-6 3-fluoro-4-(7-hydroxyisoquinolin-3-yl)benzoic acid 
• 1383379-89-2 3-fluoro-4-(7-methoxyisoquinolin-3-yl)benzoic acid 
• 1334303-21-7 {4-[(4-{3-(cyanomethyl)-3-[4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]azetidin-1-yl}piperidin-1-yl)carbonyl]-2-fluorophenyl}boronic acid 
• 1258878-95-3 4-(5-bromopyridin-2-yl)-3-fluorobenzoic acid 

Relevant articles and documents

Ortho-substituted aryl monoboronic acids have improved selectivity for d-glucose relative to d-fructose and l-lactate

Ortho-substituted aryl monoboronic acids have been found to have improved selectivity for d-glucose compared to d-fructose and l-lactate. These findings are supported by computational studies on the B3LYP/6-31G(d) level using Gaussian. This finding is of