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Catalog Number:
39895
CAS Number:
922706-40-9
2-(9H-Fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
9H-Fluorene-2-boronic acid pinacol ester, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)-9H-fluorene
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$133.30 /5G
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Product Information

2-(9H-Fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound that has garnered attention in various fields, particularly in organic synthesis and materials science. Its unique structure, featuring a fluorenyl group, enhances its reactivity and stability, making it an excellent candidate for applications in the development of advanced materials and pharmaceuticals. This compound is particularly useful in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds, thereby facilitating the synthesis of complex organic molecules.

Researchers and industry professionals can leverage this compound for the creation of novel polymers, organic light-emitting diodes (OLEDs), and other electronic materials due to its favorable electronic properties. Additionally, its ability to act as a boron source in various chemical transformations positions it as a valuable tool in synthetic chemistry. With its distinctive features, 2-(9H-Fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a critical component for innovative research and development in both academic and industrial settings.

Synonyms
9H-Fluorene-2-boronic acid pinacol ester, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)-9H-fluorene
CAS Number
922706-40-9
Purity
≥ 98% (GC)
Molecular Formula
C19H21BO2
Molecular Weight
292.19
MDL Number
MFCD16294548
PubChem ID
56925000
Melting Point
76 - 80 ?C
Appearance
White to orange crystalline powder
Conditions
Store at RT
General Information
Synonyms
9H-Fluorene-2-boronic acid pinacol ester, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)-9H-fluorene
CAS Number
922706-40-9
Purity
≥ 98% (GC)
Molecular Formula
C19H21BO2
Molecular Weight
292.19
MDL Number
MFCD16294548
PubChem ID
56925000
Melting Point
76 - 80 ?C
Appearance
White to orange crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(9H-Fluoren-2-yl)-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 essential for creating complex molecules in pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a crucial role in the development of new drug candidates by acting as a building block in the synthesis of biologically active compounds, enhancing the efficiency of drug discovery processes.
  • Materials Science: The compound is used in the fabrication of advanced materials, including polymers and nanomaterials, which are vital for electronics, coatings, and other high-performance applications.
  • Analytical Chemistry: It is employed in the preparation of samples for analytical techniques, improving the detection and quantification of various substances in environmental and biological samples.
  • Research and Development: This chemical is a key component in various research projects, enabling scientists to explore new chemical reactions and mechanisms, thus driving innovation in multiple scientific fields.

Citations