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Catalog Number:
39950
CAS Number:
1009033-83-3
4-[3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]pyridine
Purity:
≥ 98% (CG)
Synonym(s):
4,4,5,5-tétraméthyl-2-[3-(4-pyridyl)phényl]-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-(4-pyridyl)phénylboronique
Documents
$137.41 /200 mg
Taille
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Product Information

4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine is a versatile compound that plays a significant role in organic synthesis and materials science. This compound is particularly valued for its unique boron-containing structure, which enhances its reactivity and stability in various chemical reactions. It is commonly utilized in the development of advanced materials, including organic light-emitting diodes (OLEDs) and organic photovoltaics, where its properties contribute to improved efficiency and performance. Additionally, its application in medicinal chemistry is noteworthy, as it serves as a building block for the synthesis of biologically active compounds, potentially leading to the discovery of new pharmaceuticals.

Researchers and industry professionals appreciate this compound for its ability to facilitate cross-coupling reactions, making it an essential tool in the synthesis of complex organic molecules. Its high stability and functional versatility allow for a wide range of applications, from drug development to the creation of innovative electronic materials. The unique characteristics of 4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine position it as a valuable asset in both academic research and industrial applications, offering significant advantages over similar compounds in terms of reactivity and stability.

Synonyms
4,4,5,5-tétraméthyl-2-[3-(4-pyridyl)phényl]-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-(4-pyridyl)phénylboronique
CAS Number
1009033-83-3
Purity
≥ 98% (CG)
Molecular Formula
C 17 H 20 BNO 2
Molecular Weight
281.16
MDL Number
MFCD20923942
PubChem ID
57416227
Melting Point
97 - 101 ?C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
4,4,5,5-tétraméthyl-2-[3-(4-pyridyl)phényl]-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-(4-pyridyl)phénylboronique
CAS Number
1009033-83-3
Purity
≥ 98% (CG)
Molecular Formula
C 17 H 20 BNO 2
Molecular Weight
281.16
MDL Number
MFCD20923942
PubChem ID
57416227
Melting Point
97 - 101 ?C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]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.
  • Fluorescent Probes: It is used to create fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time, which is crucial in drug discovery and development.
  • Material Science: The compound finds applications in the development of advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength.
  • Chemical Sensors: It is incorporated into chemical sensors for detecting environmental pollutants, providing a reliable method for monitoring air and water quality.
  • Medicinal Chemistry: The compound plays a role in designing new therapeutic agents, particularly in targeting specific biological pathways, which can lead to more effective treatments with fewer side effects.

Citations