1150561-72-0

Basic information

• Product Name: 2-Morpholinopyridine-3-boronic acid, pinacol ester
• Synonyms: 2-Morpholinopyridine-3-boronic acid, pinacol ester;4-(3-(4,4,5,5-TetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)Morpholine;4-[3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]morpholine
• CAS NO: 1150561-72-0
• Molecular Formula: C15H23BN2O3
• Molecular Weight: 290.17
• Mol File: 1150561-72-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 472.922 °C at 760 mmHg
• Flash Point: 239.815 °C
• Appearance: /
• Density: 1.167 g/cm³
• CAS DataBase Reference: 2-Morpholinopyridine-3-boronic acid, pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Morpholinopyridine-3-boronic acid, pinacol ester(1150561-72-0)
• EPA Substance Registry System: 2-Morpholinopyridine-3-boronic acid, pinacol ester(1150561-72-0)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 1150561-72-0(Hazardous Substances Data)

Usage

General Description

2-Morpholinopyridine-3-boronic acid, pinacol ester is a boronic acid derivative used in organic synthesis as a building block for various organic molecules. It is commonly used as a reagent in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds, which is a valuable tool in the synthesis of complex organic molecules. 2-Morpholinopyridine-3-boronic acid, pinacol ester possesses a boronic acid functional group, which is known to be a versatile moiety for the formation of covalent bonds with other molecules. Additionally, the pinacol ester group provides stability and solubility to the molecule, making it a useful reagent for a variety of organic transformations. This chemical compound is commonly used in medicinal and agrochemical research as well as in the pharmaceutical industry for the synthesis of bioactive compounds.