745784-11-6

Basic information

• Product Name: (4-FLUOROQUINOLIN-3-YL)BORONIC ACID
• Synonyms: 4-FLUOROQUINOLINE-3-BORONIC ACID;(4-FLUOROQUINOLIN-3-YL)BORONIC ACID;3-Borono-4-fluoroquinoline, 3-Borono-4-fluoro-1-azanaphthalene
• CAS NO: 745784-11-6
• Molecular Formula: C9H7BFNO2
• Molecular Weight: 190.97
• Mol File: 745784-11-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 400.4±55.0 °C(Predicted)
• Appearance: /
• Density: 1.37±0.1 g/cm3(Predicted)
• PKA: 3.34±0.30(Predicted)
• CAS DataBase Reference: (4-FLUOROQUINOLIN-3-YL)BORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (4-FLUOROQUINOLIN-3-YL)BORONIC ACID(745784-11-6)
• EPA Substance Registry System: (4-FLUOROQUINOLIN-3-YL)BORONIC ACID(745784-11-6)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 745784-11-6(Hazardous Substances Data)

Usage

Description

(4-Fluoroquinolin-3-yl)boronic acid is a chemical compound that belongs to the class of boronic acids. It is characterized by a boronic acid group attached to a 4-fluoroquinolin-3-yl ring, which provides it with unique structural and reactivity properties. (4-FLUOROQUINOLIN-3-YL)BORONIC ACID is known for its ability to form stable complexes with diols and other multifunctional molecules, making it a versatile building block in various chemical reactions.

Uses

Used in Pharmaceutical Synthesis:
(4-Fluoroquinolin-3-yl)boronic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity enable the development of new drugs with potential applications in treating a wide range of diseases and medical conditions.
Used in Agrochemical Development:
In the agrochemical industry, (4-Fluoroquinolin-3-yl)boronic acid is utilized as a starting material for the creation of novel compounds with pesticidal, herbicidal, or fungicidal properties. Its incorporation into these compounds can lead to enhanced efficacy and selectivity, ultimately contributing to more effective and environmentally friendly agricultural practices.
Used in Organic Chemistry:
(4-Fluoroquinolin-3-yl)boronic acid is employed as a reagent in organic chemistry for a variety of purposes. Its ability to form stable complexes with diols and other multifunctional molecules makes it a valuable tool in the synthesis of complex organic compounds, including those with potential applications in materials science, electronics, and other advanced technologies.
Used in Medicinal Chemistry and Drug Development:
Due to its unique structure and reactivity, (4-Fluoroquinolin-3-yl)boronic acid has potential applications in medicinal chemistry and drug development. Researchers can leverage its properties to design and synthesize new drug candidates with improved pharmacological profiles, potentially leading to the discovery of innovative treatments for various diseases and conditions.