1704067-30-0

Basic information

• Product Name: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid
• Synonyms: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid
• CAS NO: 1704067-30-0
• Molecular Formula: C11H13BF3NO2
• Molecular Weight: 259.0326296
• Mol File: 1704067-30-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 411.5±55.0 °C(Predicted)
• Appearance: /
• Density: 1.34±0.1 g/cm3(Predicted)
• PKA: 7.58±0.10(Predicted)
• CAS DataBase Reference: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid(1704067-30-0)
• EPA Substance Registry System: (3-(pyrrolidin-1-yl)-5-(trifluoroMethyl)phenyl)boronic acid(1704067-30-0)

Safety Data

• Hazardous Substances Data: 1704067-30-0(Hazardous Substances Data)

Usage

Description

(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is a chemical compound that plays a significant role in organic synthesis and pharmaceutical research. It features a boronic acid group, which is instrumental in Suzuki coupling reactions for the formation of carbon-carbon bonds. The incorporation of a trifluoromethyl group imparts distinctive properties to the molecule, enhancing its utility in the creation of innovative drugs and agrochemicals. The pyrrolidin-1-yl group present in the compound indicates its potential as a building block in the synthesis of biologically active molecules. In essence, (3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is a multifaceted and beneficial chemical entity that significantly contributes to the progress of organic chemistry and drug discovery.

Uses

Used in Organic Synthesis:
(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structural features facilitate the development of new synthetic pathways and methodologies.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is employed as a building block for the synthesis of biologically active compounds. Its presence in drug candidates can potentially lead to the discovery of new therapeutic agents with improved pharmacological properties.
Used in Drug Development:
(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is used as a structural component in the development of novel drugs and agrochemicals. The trifluoromethyl group adds specific characteristics that can enhance the potency, selectivity, and metabolic stability of the resulting compounds.
Used in Suzuki Coupling Reactions:
As a boronic acid derivative, (3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid is used as a coupling partner in Suzuki reactions to form carbon-carbon bonds. This application is crucial for the assembly of complex molecular frameworks and the synthesis of diverse organic compounds.