1704064-21-0

Basic information

• Product Name: (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid
• Synonyms: (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid
• CAS NO: 1704064-21-0
• Molecular Formula: C13H19BFNO2
• Molecular Weight: 251.1048632
• Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate
• Mol File: 1704064-21-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 370.0±52.0 °C(Predicted)
• Appearance: /
• Density: 1.16±0.1 g/cm3(Predicted)
• PKA: 8.22±0.58(Predicted)
• CAS DataBase Reference: (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid(1704064-21-0)
• EPA Substance Registry System: (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid(1704064-21-0)

Safety Data

• Hazardous Substances Data: 1704064-21-0(Hazardous Substances Data)

Usage

Description

(2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is a boronic acid derivative that features a fluorine atom, a piperidine ring, and a boronic acid moiety. It is widely recognized for its role in organic synthesis and medicinal chemistry, where it serves as a reagent to facilitate the creation of carbon-carbon and carbon-heteroatom bonds.

Uses

Used in Pharmaceutical Development:
(2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is used as a key reagent in pharmaceutical development for its ability to selectively bind to specific target molecules. This selective binding makes it a valuable tool in drug discovery and development processes, contributing to the advancement of new medications.
Used in Agrochemical Production:
In the agrochemical industry, (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is utilized as an intermediate in the synthesis of various agrochemicals. Its capacity to form essential bonds allows for the creation of effective compounds used in agricultural applications.
Used in Materials Science:
(2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is employed in materials science for its potential to contribute to the development of new materials with unique properties. Its role in bond formation can lead to the engineering of materials with specific characteristics for various applications.
Used in Catalysis:
As a component in catalytic processes, (2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is used to enhance the efficiency of chemical reactions. Its presence can improve the rate of reactions and selectivity, making it a useful agent in the field of catalysis.
Used in Imaging Techniques:
(2-fluoro-4-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid has potential applications in imaging techniques, where its unique structure and bonding capabilities can be harnessed to develop new imaging agents or enhance existing ones, contributing to advancements in diagnostic and research imaging.