Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40285
CAS Number:
909709-42-8
3-Fluoro-4'-propyl-4-biphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4'-Propyl-3-fluoro-4-biphenyl boronic acid
Documents
$100.05 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-Fluoro-4'-propyl-4-biphenylboronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its application extends to the development of pharmaceuticals, particularly in the synthesis of biologically active compounds and agrochemicals. Researchers value this compound for its effectiveness in enhancing the selectivity and efficiency of chemical reactions, which can lead to the creation of novel therapeutic agents.

Additionally, 3-Fluoro-4'-propyl-4-biphenylboronic acid is beneficial in materials science, where it can be utilized in the fabrication of advanced materials with tailored properties. Its unique fluorine substitution enhances its reactivity and solubility, making it an attractive choice for various applications. With its growing importance in both research and industrial settings, this compound stands out as a key player in the ongoing development of innovative chemical processes and products.

Synonyms
4'-Propyl-3-fluoro-4-biphenyl boronic acid
CAS Number
909709-42-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C15H16BFO2
Molecular Weight
258.1
MDL Number
MFCD10687198
PubChem ID
53402576
Appearance
White to slightly yellow crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4'-Propyl-3-fluoro-4-biphenyl boronic acid
CAS Number
909709-42-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C15H16BFO2
Molecular Weight
258.1
MDL Number
MFCD10687198
PubChem ID
53402576
Appearance
White to slightly yellow crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Fluoro-4'-propyl-4-biphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, enhancing the efficacy of drug formulations.
  • Organic Electronics: It is used in the fabrication of organic light-emitting diodes (OLEDs) and organic photovoltaics, contributing to advancements in energy-efficient display technologies and solar cells.
  • Chemical Sensors: The compound is effective in creating sensors for detecting specific biomolecules, which can be crucial in medical diagnostics and environmental monitoring.
  • Cross-Coupling Reactions: It plays a significant role in Suzuki-Miyaura coupling reactions, facilitating the formation of carbon-carbon bonds in organic synthesis, which is essential for creating complex organic molecules.
  • Material Science: This chemical is employed in the development of advanced materials, including polymers and nanocomposites, which have applications in various industries such as automotive and aerospace.

Citations