1704073-49-3

Basic information

• Product Name: (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid
• Synonyms: (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid;(3-fluoro-5-(4-Methylpiperidin-1-yl)phenyl)boronic acid
• CAS NO: 1704073-49-3
• Molecular Formula: C11H16BFN2O2
• Molecular Weight: 238.0663432
• Mol File: 1704073-49-3.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 428.7±55.0 °C(Predicted)
• Appearance: /
• Density: 1.26±0.1 g/cm3(Predicted)
• PKA: 7.60±0.10(Predicted)
• CAS DataBase Reference: (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid(1704073-49-3)
• EPA Substance Registry System: (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid(1704073-49-3)

Safety Data

• Hazardous Substances Data: 1704073-49-3(Hazardous Substances Data)

Usage

Description

(3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid is a boronic acid derivative with the molecular formula C11H14BFNO2. It features a fluorine atom and a methylpiperazine group, which contribute to its unique chemical properties. (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid is known for its potential applications in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its specific uses and properties may be further explored through research and development in the fields of medicinal chemistry and materials science.

Uses

Used in Organic Synthesis:
(3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid is used as a synthetic building block for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows for versatile reactions in organic synthesis, enabling the creation of complex molecules and compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid may be employed as a key intermediate in the development of new pharmaceutical compounds. Its ability to form stable bonds with other molecules can contribute to the design of novel drugs with improved efficacy and selectivity.
Used in Materials Science:
(3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid has potential applications in materials science, where its unique properties can be utilized to develop new materials with specific characteristics. Its ability to form stable bonds can be leveraged to create materials with enhanced properties, such as improved stability, reactivity, or selectivity.
Used in Research and Development:
As a chemical compound with potential applications in various fields, (3-fluoro-5-(4-Methylpiperazin-1-yl)phenyl)boronic acid is used in research and development to explore its specific uses and properties. Further studies can uncover its potential in different industries, leading to the development of innovative products and technologies.