629644-82-2

Basic information

• Product Name: QUINOLIN-7-YLBORONIC ACID
• Synonyms: quinolin-7-yl-7-boronic acid;7-Boronoquinoline;Boronic acid, 7-quinolinyl-;7-Quinolinylboronic acid;B-7-Quinolinylboronic acid;Boronic acid, B-7-quinolinyl-;QUINOLIN-7-YLBORONIC ACID;Quinoline-7-boronic acid
• CAS NO: 629644-82-2
• Molecular Formula: C₉H₈BNO₂
• Molecular Weight: 172.98
• EINECS: -0
• Mol File: 629644-82-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 400.3±37.0 °C(Predicted)
• Appearance: /
• Density: 1.28
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 7.43±0.30(Predicted)
• CAS DataBase Reference: QUINOLIN-7-YLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: QUINOLIN-7-YLBORONIC ACID(629644-82-2)
• EPA Substance Registry System: QUINOLIN-7-YLBORONIC ACID(629644-82-2)

Safety Data

• Hazardous Substances Data: 629644-82-2(Hazardous Substances Data)

Usage

Description

Quinolin-7-ylboronic acid, an organoboron compound with the chemical formula C9H8BNO2, is a boronic acid derivative featuring a quinoline ring, a heterocyclic aromatic compound. This versatile chemical is widely recognized for its ability to form stable covalent bonds with various functional groups, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and materials. Additionally, its role as a reagent in organic synthesis, participating in cross-coupling reactions to form C-C and C-N bonds, further underscores its importance in the chemical industry.

Uses

Used in Pharmaceutical Industry:
Quinolin-7-ylboronic acid is used as a key building block for the synthesis of various pharmaceuticals, leveraging its capacity to form stable covalent bonds with different functional groups. This property allows for the creation of a wide range of drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Quinolin-7-ylboronic acid serves as a crucial component in the development of new agrochemicals. Its reactivity and ability to form stable bonds contribute to the design of effective and targeted pest control agents.
Used in Material Science:
Quinolin-7-ylboronic acid is utilized as a versatile reagent in material science. Its involvement in cross-coupling reactions to form C-C and C-N bonds is essential for the synthesis of advanced materials with specific properties for various applications.
Used in Organic Synthesis:
As a reagent in organic synthesis, Quinolin-7-ylboronic acid is used to facilitate various cross-coupling reactions. These reactions are fundamental in constructing complex organic molecules, which are vital for the development of new chemical entities in research and industry.

Upstream product

• 25334-12-7 7-iodoquinoline 

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