1310383-43-7

Basic information

• Product Name: 2,3-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
• Synonyms: 2,3-Dimethyl-2H-indazole-4-boronic acid, pinacol ester;2,3-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole;2,3-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole, 2-(2,3-Dimethyl-2H-indazol-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2,3-dimethyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
• CAS NO: 1310383-43-7
• Molecular Formula: C15H21BN2O2
• Molecular Weight: 272.15044
• Mol File: 1310383-43-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole(1310383-43-7)
• EPA Substance Registry System: 2,3-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole(1310383-43-7)

Safety Data

• Hazardous Substances Data: 1310383-43-7(Hazardous Substances Data)

Usage

General Description

2,3-Dimethyl-2H-indazole-4-boronic acid pinacol ester is a chemical compound used in organic synthesis as a reagent for the Suzuki-Miyaura coupling reaction, which is widely used in the pharmaceutical and agrochemical industries. 2,3-Dimethyl-2H-indazole-4-boronic acid pinacol ester is a boronic acid derivative, containing a boron atom bonded to a pinacol ester and an indazole ring with two methyl groups attached to it. It is a versatile building block for the synthesis of pharmaceuticals, natural products, and other organic compounds. It is also used as a tool in chemical biology research, particularly in the development of small molecule inhibitors and chemical probes for studying biological processes.