1704080-71-6

Basic information

• Product Name: (4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride
• Synonyms: (4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride;(4-(3-(DIMETHYLAMINO)PROPOXY)-3-FLUOROPHENYL)BORONIC ACID HCL
• CAS NO: 1704080-71-6
• Molecular Formula: C11H18BClFNO3
• Molecular Weight: 277.5279232
• Mol File: 1704080-71-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride(1704080-71-6)
• EPA Substance Registry System: (4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride(1704080-71-6)

Safety Data

• Hazardous Substances Data: 1704080-71-6(Hazardous Substances Data)

Usage

Description

(4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride is a boronic acid derivative used in organic synthesis and medicinal chemistry. It is a valuable reagent for the Suzuki-Miyaura cross-coupling reaction, a widely used method to form carbon-carbon bonds. The presence of the hydrochloride group in the compound indicates that it is a salt form of the boronic acid, which may make it more stable and easier to handle in certain reactions.

Uses

Used in Organic Synthesis:
(4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride is used as a reagent for the Suzuki-Miyaura cross-coupling reaction, which is a widely used method to form carbon-carbon bonds. This reaction is important in the synthesis of various organic compounds, including pharmaceuticals and materials.
Used in Medicinal Chemistry:
(4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride is used as a building block in the development of new pharmaceuticals. Its unique structure and reactivity make it a valuable tool for medicinal chemists working on drug discovery.
Used in Materials Science:
(4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride may be used in the development of new materials with specific properties, such as conductivity or stability. Its reactivity and ability to form carbon-carbon bonds make it a useful component in the synthesis of advanced materials.
Used in Chemical Biology:
(4-(3-(diMethylaMino)propoxy)-3-fluorophenyl)boronic acid hydrochloride may be of interest to researchers in chemical biology, as it can be used to study the interactions between small molecules and biological targets. Its unique structure and reactivity can provide insights into the mechanisms of biological processes and the development of new therapeutic agents.