693232-06-3

Basic information

• Product Name: 2-BroMo-3-hydroxybenzonitrile
• Synonyms: 2-BroMo-3-hydroxybenzonitrile;2-Bromo-3-hydroxybenzonitrle
• CAS NO: 693232-06-3
• Molecular Formula: C7H4BrNO
• Molecular Weight: 198.01676
• Mol File: 693232-06-3.mol

Chemical Properties

• Boiling Point: 284℃
• Flash Point: 125℃
• Appearance: /
• Density: 1.79
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-BroMo-3-hydroxybenzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BroMo-3-hydroxybenzonitrile(693232-06-3)
• EPA Substance Registry System: 2-BroMo-3-hydroxybenzonitrile(693232-06-3)

Safety Data

• Hazardous Substances Data: 693232-06-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Synthesis:
2-Bromo-3-hydroxybenzonitrile is used as an intermediate in the synthesis of pharmaceuticals for its ability to participate in various reactions, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 2-Bromo-3-hydroxybenzonitrile is utilized as a building block in the creation of compounds that have applications in crop protection and pest control, enhancing agricultural productivity.
Used in Organic Synthesis:
2-Bromo-3-hydroxybenzonitrile is used as a versatile intermediate in organic synthesis, allowing for the formation of a wide range of aromatic compounds and other fine chemicals, which are essential in various industrial applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Bromo-3-hydroxybenzonitrile is employed for its potential in the development of functional organic materials that can be used in drug discovery and the design of novel therapeutic agents.
Used in Laboratory Research:
Due to its relatively low toxicity, 2-Bromo-3-hydroxybenzonitrile is considered a safer compound to handle in laboratory settings, making it suitable for use in research and development projects that require its unique reactivity and properties.

Upstream product

• 873-62-1 m-cyanophenol 

Relevant articles and documents

Regioselective electrophilic aromatic bromination: Theoretical analysis and experimental verification

Electrophilic aromatic bromination is the most common synthetic method used to prepare aryl bromides, which are very useful intermediates in organic synthesis. To understand the experimental results in electrophilic aromatic brominations, ab initio calculations are used here for a tentative analysis of the positional selectivity. The calculated results agree well with the corresponding experimental data, and the reliability of the resulting positional selectivity was verified by the corresponding experimental data.

Synthesis of benzyloxycyanophenylboronic esters

The synthesis of six new benzyloxycyanoboronic esters: 2-benzyloxy-6- cyanophenyl-4,4,5,5-tetramethyl-[1,3,2]-dioxaborolane (4a), 4-benzyloxy-2- cyanophenyl-4,4,5, 5-tetramethyl-[1,3,2]dioxaborolane (4b), 4-benzyloxy-3- cyanophenyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (8a), 2-benzyloxy-5- cyanophenyl-4,4,5,5-tetramethyl-[1,3,2]-dioxaborolane (8b), 3-benzyloxy-4- cyanophenyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (12a), and 2-benzyloxy-5-cyanophenyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (12b) is reported. Copyright by Walter de Gruyter Berlin Boston.

Synthesis of Benzyloxybromobenzonitriles

The synthesis of four new benzyloxybromobenzonitriles including: 2-benzyloxy-4-bromobenzonitrile (3), 3-benzyloxy-4-bromobenzonitrile (7), 5-benzyloxy-2-bromobenzonitrile (11) and 3-benzyloxy-2-bromobenzonitrile (12) is reported.