1051316-38-1

Basic information

• Product Name: (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid
• Synonyms: (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid;B-(2,3-dihydro-2-oxo-1H-indol-5-yl)-boronic acid;(2-Oxoindolin-5-yl)boronic acid;(2-oxo-1,3-dihydroindol-5-yl)boronic acid;Oxindole-5-boronic acid
• CAS NO: 1051316-38-1
• Molecular Formula: C₈H₈BNO₃
• Molecular Weight: 176.96502
• Mol File: 1051316-38-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid(1051316-38-1)
• EPA Substance Registry System: (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid(1051316-38-1)

Safety Data

• Hazardous Substances Data: 1051316-38-1(Hazardous Substances Data)

Usage

Description

(2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid is a chemical compound with the molecular formula C8H8BNO3. It is a boronic acid derivative of an indole compound, characterized by a boronic acid functional group attached to the indole ring. (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid is known for its versatility in organic synthesis, making it a valuable component in various chemical reactions.

Uses

Used in Pharmaceutical Synthesis:
(2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid is used as a synthetic intermediate for the development of pharmaceuticals. Its unique structure and reactivity allow for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid is utilized as a key component in the synthesis of novel agrochemicals. Its ability to participate in various chemical reactions facilitates the design of innovative compounds for crop protection and enhancement of agricultural productivity.
Used in Material Science:
(2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid is employed as a building block in the synthesis of new materials. Its reactivity in cross-coupling reactions contributes to the development of advanced materials with specific properties for use in various industries.
Used in Organic Synthesis:
As a versatile boronic acid derivative, (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid is used in organic synthesis for the formation of new organic compounds. Its participation in Suzuki-Miyaura coupling reactions and other cross-coupling reactions enables the synthesis of complex organic molecules with diverse applications.
Further research and exploration of the properties and reactivity of (2-oxo2,3-dihydro-1H-indol-5-yl)boronic acid in various chemical reactions may reveal additional uses and benefits, expanding its applications across different industries.