1309601-94-2

Basic information

• Product Name: 5-(HYDROXYMETHYL)PYRIDINE-2-BORONIC ACID PINACOL ESTER
• Synonyms: 5-(HYDROXYMETHYL)PYRIDINE-2-BORONIC ACID PINACOL ESTER;(6-(4,4,5,5-TetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)Methanol
• CAS NO: 1309601-94-2
• Molecular Formula: C12H18BNO3
• Molecular Weight: 235.09
• Mol File: 1309601-94-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 377.1±32.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 13.73±0.10(Predicted)
• CAS DataBase Reference: 5-(HYDROXYMETHYL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(HYDROXYMETHYL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(1309601-94-2)
• EPA Substance Registry System: 5-(HYDROXYMETHYL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(1309601-94-2)

Safety Data

• Hazardous Substances Data: 1309601-94-2(Hazardous Substances Data)

Usage

General Description

"(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methanol" is a chemical compound that is commonly used as a reagent in organic synthesis. It consists of a pyridine ring attached to a boron-containing heterocycle, with a methanol group attached to the pyridine ring. (6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methanol has been utilized in various reactions, including Suzuki-Miyaura cross-coupling reactions, which are important in the synthesis of complex organic molecules. The boron atom in the compound makes it particularly useful in forming carbon-carbon bonds, and its unique structure allows for selective functionalization of the pyridine ring. Additionally, this compound has potential applications in the development of pharmaceuticals and other fine chemicals.