Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
39933
CAS Number:
193978-23-3
2-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)tiofeno
Purity:
≥ 98% (GC)
Synonym(s):
4,4,5,5-Tetrametil-2-(2-tienil)-1,3,2-dioxaborolano, Éster de pinacol del ácido 2-tiofenoborónico
Documents
$20.63 /1G
Tamaño
Request Bulk Quote
Product Information

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a versatile compound that combines the unique properties of dioxaborolane with the aromatic characteristics of thiophene. This compound is particularly valuable in organic synthesis and materials science, where it serves as a building block for the development of advanced materials, including organic semiconductors and photovoltaic devices. Its structure allows for enhanced stability and solubility, making it an excellent candidate for applications in electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).

Researchers and industry professionals can leverage the unique reactivity of this compound to create functionalized materials with tailored properties, facilitating innovations in electronics and optoelectronics. Its ability to form stable complexes with various substrates also opens avenues for catalysis and sensor applications. With its promising potential in cutting-edge technologies, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene stands out as a key component for those looking to push the boundaries of material science and organic chemistry.

Synonyms
4,4,5,5-Tetrametil-2-(2-tienil)-1,3,2-dioxaborolano, Éster de pinacol del ácido 2-tiofenoborónico
CAS Number
193978-23-3
Purity
≥ 98% (GC)
Molecular Formula
C10H15BO2S
Molecular Weight
210.1
MDL Number
MFCD05663878
PubChem ID
10703628
Melting Point
66 - 70 ?C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar a ≤ -10 °C
General Information
Synonyms
4,4,5,5-Tetrametil-2-(2-tienil)-1,3,2-dioxaborolano, Éster de pinacol del ácido 2-tiofenoborónico
CAS Number
193978-23-3
Purity
≥ 98% (GC)
Molecular Formula
C10H15BO2S
Molecular Weight
210.1
MDL Number
MFCD05663878
PubChem ID
10703628
Melting Point
66 - 70 ?C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar a ≤ -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Electronics: This compound is used in the development of organic semiconductors, which are crucial for creating efficient organic light-emitting diodes (OLEDs) and organic photovoltaic cells. Its unique structure enhances charge transport properties, leading to better performance in electronic devices.
  • Fluorescent Probes: It serves as a building block for synthesizing fluorescent probes used in biological imaging. These probes help researchers visualize cellular processes in real-time, providing insights into disease mechanisms and drug interactions.
  • Catalysis: The compound plays a role in catalytic processes, particularly in cross-coupling reactions. Its boron-containing structure can improve reaction efficiency and selectivity, making it valuable in synthetic organic chemistry.
  • Material Science: It is employed in the formulation of advanced materials, such as polymers and composites, that require specific electrical or optical properties. This application is particularly relevant in the development of lightweight and durable materials for automotive and aerospace industries.
  • Pharmaceutical Development: The compound is explored for its potential in drug discovery, particularly in creating new therapeutic agents. Its unique chemical properties may lead to the development of novel drugs with improved efficacy and reduced side effects.

Citas