1190875-60-5

Basic information

• Product Name: (2-chloro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)Methanol
• Synonyms: (2-chloro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)Methanol;3-Chloro-4-(hydroxymethyl)phenylboronic acid
• CAS NO: 1190875-60-5
• Molecular Formula: C13H18BClO3
• Molecular Weight: 268.54422
• EINECS: -0
• Mol File: 1190875-60-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-chloro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-chloro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)Methanol(1190875-60-5)
• EPA Substance Registry System: (2-chloro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)Methanol(1190875-60-5)

Safety Data

• Hazardous Substances Data: 1190875-60-5(Hazardous Substances Data)

Usage

General Description

3-Chloro-4-(hydroxymethyl)phenylboronic acid is a chemical compound with the molecular formula C7H8BClO3. It is a boronic acid derivative that contains a chloro group and a hydroxymethyl group on a phenyl ring. 3-Chloro-4-(hydroxymethyl)phenylboronic acid is used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It is also a versatile building block in the preparation of pharmaceuticals and agrochemicals. Additionally, 3-Chloro-4-(hydroxymethyl)phenylboronic acid has potential applications in material science and bioconjugation chemistry due to its ability to bind to various biomolecules and surfaces. Overall, this compound plays a significant role in the field of organic chemistry and has diverse applications in various industries.