1704080-68-1

Basic information

• Product Name: (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid
• Synonyms: (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid
• CAS NO: 1704080-68-1
• Molecular Formula: C13H19BClNO2
• Molecular Weight: 267.55946
• Mol File: 1704080-68-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid(1704080-68-1)
• EPA Substance Registry System: (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid(1704080-68-1)

Safety Data

• Hazardous Substances Data: 1704080-68-1(Hazardous Substances Data)

Usage

Description

(4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is a boronic acid derivative with the molecular formula C13H18BClNO2. It is characterized by the presence of a boron atom bound to a phenyl ring and a chlorine atom. (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid also features a piperidine ring with a methyl group attached to it, which may suggest potential activity as a ligand for certain biological targets. Due to its unique structure and properties, it holds significance in the field of organic chemistry and may find applications in pharmaceutical research and development.

Uses

Used in Pharmaceutical Research and Development:
(4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is used as a chemical compound in pharmaceutical research and development for its potential activity as a ligand for certain biological targets. The presence of the piperidine group in this compound may allow it to interact with specific receptors or enzymes, making it a promising candidate for the development of new drugs or therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is used as a boronic acid derivative for its ability to form stable complexes with diols and certain other molecules. This property can be exploited in various chemical reactions and synthesis processes, contributing to the development of new compounds and materials.
Used in Chemical Synthesis:
(4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid is used as a key intermediate in the synthesis of various complex organic molecules. Its unique structure, which includes a boron atom and a phenyl ring, allows it to participate in a range of chemical reactions, making it a valuable building block for the creation of novel compounds with potential applications in various industries.
Used in Material Science:
In material science, (4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid may be used as a component in the development of new materials with specific properties. Its ability to form stable complexes with other molecules could be utilized to create materials with enhanced characteristics, such as improved stability, reactivity, or selectivity, depending on the desired application.
Used in Analytical Chemistry:
(4-chloro-3-((4-Methylpiperidin-1-yl)Methyl)phenyl)boronic acid can be employed as a reagent or a reference compound in analytical chemistry. Its unique structure and properties may be useful for the development of new analytical methods or the improvement of existing ones, contributing to the advancement of chemical analysis techniques.