1288978-82-4

Basic information

• Product Name: 1,3,2-dioxaborolane,2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetraMethyl-
• Synonyms: 1,3,2-dioxaborolane,2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetraMethyl-;2-(4-Fluoro-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;4-Fluoro-2-nitrobenzeneboronic acid pinacol ester, 96%
• CAS NO: 1288978-82-4
• Molecular Formula: C₁₂H₁₅BFNO₄
• Molecular Weight: 267.0612032
• Mol File: 1288978-82-4.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 354.4±32.0 °C(Predicted)
• Appearance: /Solid
• Density: 1.20±0.1 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1,3,2-dioxaborolane,2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetraMethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,2-dioxaborolane,2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetraMethyl-(1288978-82-4)
• EPA Substance Registry System: 1,3,2-dioxaborolane,2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetraMethyl-(1288978-82-4)

Safety Data

• Hazardous Substances Data: 1288978-82-4(Hazardous Substances Data)

Usage

General Description

1,3,2-Dioxaborolane, 2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetramethyl- is a chemical compound often used in organic synthesis and as a reagent in various reactions. It is a boronic ester with a tetramethyl substitution at the 4 and 5 positions, as well as a 4-fluoro-2-nitrophenyl group at the 2 position. 1,3,2-Dioxaborolane,2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetramethyl- is often used in palladium-catalyzed cross-coupling reactions, where it serves as a source of the tetramethyl boron group. It has also been utilized in the synthesis of pharmaceutical compounds and materials science applications. Overall, 1,3,2-Dioxaborolane, 2-(4-fluoro-2-nitrophenyl)-4,4,5,5-tetramethyl- is an important and versatile compound in the field of organic chemistry.

Downstream Products

• 1288977-88-7 (1S,2R,3R)-1-[5-(4-fluoro-2-nitrophenyl)thiophene-2-sulfonylamino]-2-methyl-3-phenylcyclopropanecarboxylic acid tert-butyl ester