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Catalog Number:
39893
CAS Number:
850881-09-3
3-Hexyl-2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)thiophène
Purity:
≥ 97% (CG)
Synonym(s):
2-(3-hexyl-2-thiényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-hexyl-2-thiophèneboronique
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Product Information

3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a versatile compound that combines the unique properties of thiophene with the stability and reactivity of a dioxaborolane moiety. This compound is particularly valuable in organic electronics, where it serves as a building block for the synthesis of advanced materials such as organic semiconductors and photovoltaic devices. Its hexyl chain enhances solubility in organic solvents, making it suitable for various applications in thin-film transistors and light-emitting diodes (LEDs).

Additionally, the presence of the dioxaborolane group allows for efficient cross-coupling reactions, facilitating the development of complex organic structures. Researchers appreciate its potential in the field of materials science, especially in the design of high-performance electronic devices. With its unique structure and properties, this compound stands out as a promising candidate for innovative applications in both academic research and industrial settings.

Synonyms
2-(3-hexyl-2-thiényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-hexyl-2-thiophèneboronique
CAS Number
850881-09-3
Purity
≥ 97% (CG)
Molecular Formula
C 16 H 27 BO 2 S
Molecular Weight
294.26
MDL Number
MFCD11045447
PubChem ID
16663552
Density
0,99 g/mL
Appearance
Liquide incolore à légèrement jaune
Refractive Index
n20D 1.49
Conditions
Magasin chez RT
General Information
Synonyms
2-(3-hexyl-2-thiényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-hexyl-2-thiophèneboronique
CAS Number
850881-09-3
Purity
≥ 97% (CG)
Molecular Formula
C 16 H 27 BO 2 S
Molecular Weight
294.26
MDL Number
MFCD11045447
PubChem ID
16663552
Density
0,99 g/mL
Appearance
Liquide incolore à légèrement jaune
Refractive Index
n20D 1.49
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-Hexyl-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 a key material in the development of organic semiconductors, which are essential for creating flexible and lightweight electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells.
  • Photovoltaic Applications: Its unique properties enhance the efficiency of solar cells, making it a valuable component in the renewable energy sector, contributing to more sustainable energy solutions.
  • Sensor Technology: The compound is used in the fabrication of chemical sensors, particularly for detecting environmental pollutants, thus aiding in environmental monitoring and protection efforts.
  • Polymer Chemistry: It serves as a building block for synthesizing advanced polymers with tailored properties, which can be applied in various industries, including packaging and automotive.
  • Research in Material Science: The compound is utilized in studies aimed at developing new materials with enhanced electrical and thermal properties, benefiting industries such as aerospace and electronics.