874289-53-9

Basic information

• Product Name: 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID
• Synonyms: 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID;5-(BENZYLCARBAMOYL)-2-FLUOROPHENYLBORONIC ACID;N-BENZYL 3-BORONO-4-FLUOROBENZAMIDE;5-(Benzylcarbamoyl)-2-fluorobenzeneboronic acid 97%;5-(Benzylcarbamoyl)-2-fluorobenzeneboronicacid97%
• CAS NO: 874289-53-9
• Molecular Formula: C14H13BFNO3
• Molecular Weight: 273.07
• Product Categories: blocks;BoronicAcids
• Mol File: 874289-53-9.mol

Chemical Properties

• Melting Point: 224-226
• Appearance: /
• Density: 1.3g/cm³
• Refractive Index: 1.595
• Storage Temp.: Keep Cold
• CAS DataBase Reference: 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID(874289-53-9)
• EPA Substance Registry System: 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID(874289-53-9)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 874289-53-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its boronic acid derivative nature makes it a valuable tool in Suzuki-Miyaura coupling reactions, a widely used method for forming carbon-carbon bonds, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID is used as a therapeutic agent for the treatment of cancer and other diseases. Its ability to selectively inhibit proteasome activity makes it a promising candidate for drug development, potentially leading to novel treatments that target specific disease pathways and improve patient outcomes.
Used in Biomedical Research:
5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID is used as a component in the development of fluorescent probes for biomolecular and cellular imaging. Its incorporation into these probes allows for the visualization and tracking of specific biological processes, providing valuable insights into cellular mechanisms and aiding in the study of disease progression and therapeutic interventions.
Overall, 5-(BENZYLCARBAMOYL)-2-FLUOROBENZENEBORONIC ACID is a versatile chemical compound with applications spanning across organic synthesis, pharmaceutical development, and biomedical research, making it an important asset in the advancement of scientific knowledge and the creation of innovative therapeutic solutions.

InChI:InChI=1/C14H13BFNO3/c16-13-7-6-11(8-12(13)15(19)20)14(18)17-9-10-4-2-1-3-5-10/h1-8,19-20H,9H2,(H,17,18)