1001200-60-7

Basic information

• Product Name: 2-(4-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 2-(4-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;4-Fluoro-3-methylphenylboronic acid, pinacol ester;4-Fluoro-3-Methylbenzeneboronic acid pinacol ester, 96%
• CAS NO: 1001200-60-7
• Molecular Formula: C13H18BFO2
• Molecular Weight: 236.0902232
• EINECS: 941-103-9
• Mol File: 1001200-60-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 303.4±35.0 °C(Predicted)
• Appearance: /Solid
• Density: 1.04g/ml
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(4-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1001200-60-7)
• EPA Substance Registry System: 2-(4-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1001200-60-7)

Safety Data

• Hazardous Substances Data: 1001200-60-7(Hazardous Substances Data)

Usage

Uses

4-Fluoro-3-methylphenylboronic acid, pinacol ester

Upstream product

• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 139911-27-6 4-fluoro-3-methylphenyl boronic acid 

Downstream Products

• 1428252-95-2 4-[4-(4-fluoro-3-methylphenyl)-1-(2-hydroxyethyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

gem-dibromomethylarenes: A convenient substitute for noncommercial aldehydes in the Knoevenagel-Doebner reaction for the synthesis of α,β-unsaturated carboxylic acids

(Chemical Equation Presented) A facile synthesis of α,β- unsaturated carboxylic acids from gem-dibromomethylarenes is described. gem-Dibromomethylarenes are employed for the first time in the Knoevenagel-Doebner reaction as aldehyde equivalents for the efficient synthesis of α,β-unsaturated carboxylic acids.