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Catalog Number:
39888
CAS Number:
144432-80-4
2-(4-Bifenilil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
Purity:
≥ 98% (GC)
Synonym(s):
4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)bifenilo, Éster de pinacol del ácido 4-bifenilborónico
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Product Information

2-(4-Biphenylyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound known for its unique structural properties that make it highly valuable in various applications. This dioxaborolane derivative features a biphenyl moiety, which enhances its stability and reactivity, making it an excellent candidate for use in organic synthesis and materials science. Its ability to act as a boron source in cross-coupling reactions is particularly noteworthy, facilitating the formation of carbon-carbon bonds in the development of complex organic molecules. Researchers in the fields of pharmaceuticals and agrochemicals have utilized this compound to create innovative products, leveraging its reactivity to produce new compounds with enhanced biological activity.

Additionally, its application in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, showcases its potential in the electronics industry. The compound's favorable properties, including thermal stability and solubility, contribute to its effectiveness in these applications. With its broad range of uses, 2-(4-Biphenylyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable tool for researchers and industry professionals seeking to push the boundaries of innovation in chemical synthesis and material development.

Synonyms
4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)bifenilo, Éster de pinacol del ácido 4-bifenilborónico
CAS Number
144432-80-4
Purity
≥ 98% (GC)
Molecular Formula
C 18 H 21 BO 2
Molecular Weight
280.17
MDL Number
MFCD07368291
PubChem ID
11989651
Melting Point
110 - 114 ?C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)bifenilo, Éster de pinacol del ácido 4-bifenilborónico
CAS Number
144432-80-4
Purity
≥ 98% (GC)
Molecular Formula
C 18 H 21 BO 2
Molecular Weight
280.17
MDL Number
MFCD07368291
PubChem ID
11989651
Melting Point
110 - 114 ?C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(4-Biphenylyl)-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 synthesizing complex organic molecules.
  • Material Science: It is employed in the development of advanced materials, particularly in creating polymers with enhanced properties, such as improved thermal stability and mechanical strength.
  • Pharmaceutical Development: The compound plays a role in drug discovery, particularly in the design of boron-containing pharmaceuticals that can enhance bioavailability and target specificity.
  • Fluorescent Probes: It is used in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high precision.
  • Electronics: This chemical is significant in the production of organic light-emitting diodes (OLEDs), contributing to the development of energy-efficient display technologies.

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