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Catalog Number:
39896
CAS Number:
406463-06-7
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin
Purity:
≥ 98% (GC)
Synonym(s):
Quinoline-6-boronic acid pinacol ester, 2-(Quinolin-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Product Information

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin is a versatile compound that has garnered attention in various fields, particularly in organic synthesis and medicinal chemistry. This compound features a unique dioxaborolane moiety, which enhances its reactivity and stability, making it an excellent candidate for cross-coupling reactions. Its application in the development of novel pharmaceuticals and agrochemicals is particularly noteworthy, as it can facilitate the formation of complex molecular architectures that are essential in drug discovery and development. Researchers have found that this compound can serve as an effective building block for synthesizing biologically active molecules, thereby streamlining the process of creating new therapeutic agents.

In addition to its synthetic utility, 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin is also recognized for its potential in materials science, particularly in the development of organic light-emitting diodes (OLEDs) and other electronic materials. Its unique properties allow for enhanced performance in these applications, making it a valuable addition to the toolkit of researchers and industry professionals alike. With its broad range of applications and the ability to facilitate innovative research, this compound stands out as a key player in advancing both scientific and industrial endeavors.

Synonyms
Quinoline-6-boronic acid pinacol ester, 2-(Quinolin-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
406463-06-7
Purity
≥ 98% (GC)
Molecular Formula
C15H18BNO2
Molecular Weight
255.12
MDL Number
MFCD06411327
PubChem ID
16217784
Melting Point
67 - 71 ?C
Appearance
White to off white crystalline powder
Conditions
Store at RT
General Information
Synonyms
Quinoline-6-boronic acid pinacol ester, 2-(Quinolin-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
406463-06-7
Purity
≥ 98% (GC)
Molecular Formula
C15H18BNO2
Molecular Weight
255.12
MDL Number
MFCD06411327
PubChem ID
16217784
Melting Point
67 - 71 ?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

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, making it valuable for chemists developing new pharmaceuticals and agrochemicals.
  • Fluorescent Probes: Its unique structure allows it to be used in creating fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Material Science: The compound is employed in the development of advanced materials, such as polymers and coatings, enhancing properties like durability and resistance to environmental factors.
  • Catalysis: It acts as a catalyst in various chemical reactions, improving efficiency and selectivity, which is crucial for industries aiming to reduce waste and energy consumption.
  • Drug Development: Researchers leverage its properties to design and optimize drug candidates, particularly in targeting specific biological pathways, which can lead to more effective treatments.

Citations