1704082-30-3

Basic information

• Product Name: (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid
• Synonyms: (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid
• CAS NO: 1704082-30-3
• Molecular Formula: C15H15BFNO4
• Molecular Weight: 303.0933032
• Mol File: 1704082-30-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid(1704082-30-3)
• EPA Substance Registry System: (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid(1704082-30-3)

Safety Data

• Hazardous Substances Data: 1704082-30-3(Hazardous Substances Data)

Usage

Description

(3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid is a boronic acid derivative that features a carboxamide group and a fluorine atom. It is widely recognized for its role as a building block in the fields of organic synthesis and medicinal chemistry.

Uses

Used in Organic Synthesis:
(3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid is used as a key component in organic synthesis for its ability to form carbon-carbon bonds through Suzuki-Miyaura coupling reactions. This capability is highly valuable for constructing complex organic molecules and expanding the scope of synthetic chemistry.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid is utilized as a pharmacophore. Its unique structure allows it to be a key element in the development of new pharmaceuticals, potentially leading to the creation of innovative treatments and therapies.
Used in Pharmaceutical Development:
(3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid is employed as a building block in the development of pharmaceuticals. Its incorporation into drug molecules can enhance their biological activity, making it a crucial component in the design of effective medications.
Used in Agrochemical Development:
Similarly, in agrochemical development, (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid is used as a building block to create new compounds for agricultural applications. Its ability to form stable bonds and its unique properties make it a valuable asset in designing effective agrochemicals.
Used as a Catalyst in Organic Reactions:
(3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid also serves as a catalyst in various organic reactions. Its catalytic properties facilitate specific transformations, making it an indispensable tool in the advancement of organic chemistry.
Used in the Modification of Biologically Active Molecules:
Lastly, (3-fluoro-5-((4-Methoxybenzyl)carbaMoyl)phenyl)boronic acid is used for the modification of biologically active molecules. Its unique structure allows for targeted enhancements, potentially improving the efficacy and selectivity of these molecules in biological systems.