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Catalog Number:
39961
CAS Number:
1115023-84-1
2-([1,1':3',1''-Terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
4,4,5,5-Tetramethyl-2-(1,1':3',1''-terphenyl)-3-yl-1,3,2-dioxaborolane, (1,1':3',1''-Terphenyl)-3-ylboronic acid pinacol ester
Documents
$36.65 /250MG
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Product Information

2-([1,1':3',1''-Terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound known for its unique structural properties that make it valuable in various applications, particularly in organic synthesis and materials science. This compound features a dioxaborolane ring, which enhances its reactivity and stability, making it an excellent candidate for use in the development of advanced materials, including organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its ability to facilitate the formation of carbon-boron bonds is particularly beneficial in cross-coupling reactions, which are essential in the synthesis of complex organic molecules.

Researchers and industry professionals can leverage this compound for its potential in creating high-performance polymers and as a building block in the synthesis of pharmaceuticals. Its unique properties allow for improved efficiency in chemical reactions, making it a preferred choice for those looking to enhance yield and reduce by-products. With its promising applications in both academic research and industrial processes, this compound stands out as a key ingredient for innovation in chemistry and materials development.

Synonyms
4,4,5,5-Tetramethyl-2-(1,1':3',1''-terphenyl)-3-yl-1,3,2-dioxaborolane, (1,1':3',1''-Terphenyl)-3-ylboronic acid pinacol ester
CAS Number
1115023-84-1
Purity
≥ 98% (GC)
Molecular Formula
C24H25BO2
Molecular Weight
356.27
MDL Number
MFCD28134531
PubChem ID
57864956
Melting Point
99 - 103 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4,4,5,5-Tetramethyl-2-(1,1':3',1''-terphenyl)-3-yl-1,3,2-dioxaborolane, (1,1':3',1''-Terphenyl)-3-ylboronic acid pinacol ester
CAS Number
1115023-84-1
Purity
≥ 98% (GC)
Molecular Formula
C24H25BO2
Molecular Weight
356.27
MDL Number
MFCD28134531
PubChem ID
57864956
Melting Point
99 - 103 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
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':3',1''-Terphenyl]-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 synthesis, particularly in cross-coupling reactions, enabling the formation of complex organic molecules efficiently.
  • Material Science: It is used in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, enhancing their performance and stability.
  • Pharmaceutical Research: The compound plays a role in drug discovery, particularly in the synthesis of boron-containing pharmaceuticals, which can improve drug efficacy and reduce side effects.
  • Fluorescent Probes: It is utilized in creating fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Catalysis: The compound acts as a catalyst in various chemical reactions, offering advantages in reaction rates and selectivity compared to traditional catalysts, thus optimizing industrial processes.

Citations