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Catalog Number:
40039
CAS Number:
912844-88-3
2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl, 3-Biphenylboronic acid pinacol ester
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Product Information

2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound known for its unique structural features that enhance its reactivity and stability. This compound is particularly valuable in organic synthesis, especially in cross-coupling reactions, where it serves as an effective boron source. Its ability to facilitate the formation of carbon-carbon bonds makes it a crucial reagent in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate its high selectivity and efficiency, which can lead to reduced reaction times and improved yields compared to traditional methods.

In addition to its synthetic applications, this compound has shown promise in the field of materials science, particularly in the development of luminescent materials and organic light-emitting diodes (OLEDs). Its unique electronic properties allow for the fine-tuning of photophysical characteristics, making it an attractive option for researchers focused on innovative electronic applications. With its broad range of uses and advantages over similar compounds, 2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable tool for both academic and industrial chemists.

Synonyms
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl, 3-Biphenylboronic acid pinacol ester
CAS Number
912844-88-3
Purity
≥ 98% (GC)
Molecular Formula
C18H21BO2
Molecular Weight
280.17
MDL Number
MFCD18452169
PubChem ID
17942655
Melting Point
80 - 84 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl, 3-Biphenylboronic acid pinacol ester
CAS Number
912844-88-3
Purity
≥ 98% (GC)
Molecular Formula
C18H21BO2
Molecular Weight
280.17
MDL Number
MFCD18452169
PubChem ID
17942655
Melting Point
80 - 84 °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

2-([1,1'-Biphenyl]-3-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, particularly in the formation of carbon-carbon bonds, making it valuable for synthesizing complex organic molecules.
  • Material Science: It is employed in the development of advanced materials, including polymers and nanomaterials, due to its unique boron-containing structure that enhances material properties.
  • Pharmaceutical Development: The compound plays a role in drug discovery, particularly in the design of boron-containing pharmaceuticals, which can improve drug efficacy and selectivity.
  • Fluorescent Probes: It is used in creating fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high precision.
  • Catalysis: This chemical acts as a catalyst in various chemical reactions, offering advantages such as increased reaction rates and improved yields compared to traditional catalysts.

Citations