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

Catalog Number:
40162
CAS Number:
214360-58-4
2-(4-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
1-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 4-Fluorophenylboronic acid pinacol ester
Documents
$72.31 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

2-(4-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound that has garnered attention for its unique properties and applications in various fields. This compound is particularly valued in organic synthesis and medicinal chemistry, where it serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential reagent for creating complex molecular architectures. Additionally, the presence of the fluorophenyl group enhances its reactivity and selectivity, allowing for the fine-tuning of chemical properties in target compounds.

Researchers and industry professionals can leverage the advantages of this compound in the synthesis of biologically active molecules, particularly in the design of targeted therapies and crop protection agents. Its stability and ease of handling further contribute to its appeal in laboratory settings. With its potential to facilitate innovative solutions in chemical research and development, 2-(4-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable tool for advancing scientific discovery and industrial applications.

Synonyms
1-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 4-Fluorophenylboronic acid pinacol ester
CAS Number
214360-58-4
Purity
≥ 98% (GC)
Molecular Formula
C12H16BFO2
Molecular Weight
222.07
MDL Number
MFCD03453665
PubChem ID
2760593
Density
1.06 g/mL
Appearance
Colorless to slightly yellow liquid
Conditions
Store at RT
General Information
Synonyms
1-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 4-Fluorophenylboronic acid pinacol ester
CAS Number
214360-58-4
Purity
≥ 98% (GC)
Molecular Formula
C12H16BFO2
Molecular Weight
222.07
MDL Number
MFCD03453665
PubChem ID
2760593
Density
1.06 g/mL
Appearance
Colorless to slightly yellow liquid
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(4-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the formation of carbon-carbon bonds, which is crucial for synthesizing complex organic molecules.
  • Medicinal Chemistry: It plays a significant role in drug development, particularly in creating compounds with enhanced biological activity and selectivity, benefiting pharmaceutical researchers.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, due to its unique chemical properties that enhance material durability and performance.
  • Fluorescent Probes: Its distinctive structure allows it to be utilized in creating fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Environmental Chemistry: This chemical is applied in the study of environmental pollutants, helping researchers develop methods for detecting and analyzing contaminants in various ecosystems.

Citations