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Catalog Number:
39932
CAS Number:
329214-79-1
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Purity:
≥ 98% (GC)
Synonym(s):
2-(3-Pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 3-Pyridylboronic acid pinacol ester
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Product Information

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound that combines the unique properties of a dioxaborolane with the aromatic characteristics of pyridine, making it a valuable tool in organic synthesis and materials science. This compound is particularly useful in the development of boron-containing ligands and catalysts, which are essential in various chemical reactions, including cross-coupling reactions that are pivotal in pharmaceutical and agrochemical industries. Its ability to stabilize reactive intermediates enhances reaction efficiency, making it a preferred choice for researchers looking to streamline synthetic pathways.

In addition to its synthetic applications, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is also explored for its potential in the development of advanced materials, including polymers and nanomaterials. The incorporation of boron into polymer matrices can significantly improve thermal stability and mechanical properties, making it ideal for high-performance applications. With its unique structure and functional properties, this compound stands out as a key ingredient for innovative research and development in various fields.

Synonyms
2-(3-Pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 3-Pyridylboronic acid pinacol ester
CAS Number
329214-79-1
Purity
≥ 98% (GC)
Molecular Formula
C11H16BNO2
Molecular Weight
205.06
MDL Number
MFCD03084758
PubChem ID
2734656
Melting Point
102 - 106 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-(3-Pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 3-Pyridylboronic acid pinacol ester
CAS Number
329214-79-1
Purity
≥ 98% (GC)
Molecular Formula
C11H16BNO2
Molecular Weight
205.06
MDL Number
MFCD03084758
PubChem ID
2734656
Melting Point
102 - 106 ?C
Appearance
White to off-white 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

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is employed in palladium-catalyzed cross-coupling reactions, which are essential for forming carbon-carbon bonds, making it valuable in materials science and drug discovery.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Ligand Development: It acts as a ligand in coordination chemistry, enhancing the stability and reactivity of metal complexes, which are crucial in catalysis and material applications.
  • Environmental Applications: This chemical can be utilized in the development of sensors for detecting environmental pollutants, providing a means for monitoring and improving environmental health.

Citations