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Catalog Number:
39978
CAS Number:
1040281-83-1
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxaldehyde
Purity:
≥ 98% (GC)
Synonym(s):
2-(5-Formyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 5-Formyl-2-thiopheneboronic acid pinacol ester
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Product Information

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxaldehyde is a versatile compound with significant applications in organic synthesis and materials science. This compound features a unique dioxaborolane moiety, which enhances its reactivity and stability, making it an excellent candidate for cross-coupling reactions and the development of advanced organic materials. Its thiophene structure contributes to its electronic properties, making it suitable for applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Researchers and industry professionals can leverage this compound for the synthesis of novel polymers and small molecules with tailored electronic properties.

In addition to its utility in organic synthesis, this compound can serve as a valuable building block in the development of agrochemicals and pharmaceuticals, where its unique functional groups can facilitate the design of new active ingredients. The combination of its stability, reactivity, and electronic characteristics positions 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxaldehyde as an essential tool for innovative research and development in various fields.

Synonyms
2-(5-Formyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 5-Formyl-2-thiopheneboronic acid pinacol ester
CAS Number
1040281-83-1
Purity
≥ 98% (GC)
Molecular Formula
C11H15BO3S
Molecular Weight
238.11
MDL Number
MFCD09266186
PubChem ID
57415686
Melting Point
66 - 70 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-(5-Formyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 5-Formyl-2-thiopheneboronic acid pinacol ester
CAS Number
1040281-83-1
Purity
≥ 98% (GC)
Molecular Formula
C11H15BO3S
Molecular Weight
238.11
MDL Number
MFCD09266186
PubChem ID
57415686
Melting Point
66 - 70 ?C
Appearance
White to light yellow 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

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

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of new pharmaceuticals and agrochemicals, enhancing efficiency in chemical reactions.
  • Material Science: It is used in the fabrication of advanced materials, including conductive polymers and organic light-emitting diodes (OLEDs), contributing to the development of next-generation electronic devices.
  • Fluorescent Probes: The compound acts as a building block for fluorescent probes, which are essential in biological imaging and diagnostics, allowing researchers to visualize cellular processes with high precision.
  • Chemical Sensors: It is employed in the creation of chemical sensors that detect environmental pollutants or biological markers, providing critical data for environmental monitoring and healthcare applications.
  • Cross-Coupling Reactions: This chemical is instrumental in cross-coupling reactions, a fundamental process in organic chemistry that allows for the formation of carbon-carbon bonds, facilitating the synthesis of complex molecules.

Citations