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Catalog Number:
26684
CAS Number:
887405-37-0
4-(3-Hydroxyprop-1-yn-1-yl)thiophene-2-carbaldehyde
Purity:
≥ 95% (NMR)
Documents
$43.87 /250MG
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Product Information

4-(3-Hydroxyprop-1-yn-1-yl)thiophene-2-carbaldehyde is a versatile compound known for its unique thiophene structure, which enhances its reactivity and application potential in various fields. This compound exhibits properties that make it particularly valuable in organic synthesis and materials science. Its hydroxyl and aldehyde functional groups allow for diverse chemical modifications, enabling researchers to create a range of derivatives tailored for specific applications.

In the realm of organic electronics, 4-(3-Hydroxyprop-1-yn-1-yl)thiophene-2-carbaldehyde can be utilized in the development of conductive polymers and organic light-emitting diodes (OLEDs), where its electron-rich thiophene ring contributes to improved charge transport properties. Additionally, its potential as a building block in the synthesis of biologically active compounds opens avenues in medicinal chemistry, particularly in the design of new pharmaceuticals. The compound's ability to undergo various reactions, such as cross-coupling and condensation, further enhances its utility in research and industrial applications, making it a valuable addition to any chemical toolkit.

CAS Number
887405-37-0
Purity
≥ 95% (NMR)
Molecular Formula
C8H6O2S
Molecular Weight
166.2
MDL Number
MFCD08059972
PubChem ID
28064043
Appearance
Brown solid
Conditions
Store at 0-8°C
General Information
CAS Number
887405-37-0
Purity
≥ 95% (NMR)
Molecular Formula
C8H6O2S
Molecular Weight
166.2
MDL Number
MFCD08059972
PubChem ID
28064043
Appearance
Brown solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(3-Hydroxyprop-1-yn-1-yl)thiophene-2-carbaldehyde is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of functionalized thiophene derivatives that are important in materials science.
  • Electronics: Its unique electronic properties make it valuable in the fabrication of organic semiconductors, which are used in devices such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells.
  • Pharmaceutical Development: The compound can be used in the design of new drug candidates, particularly those targeting specific biological pathways, due to its potential bioactivity.
  • Sensor Technology: It is employed in the creation of chemical sensors, leveraging its ability to interact with various analytes, thus enhancing detection methods in environmental monitoring.
  • Research in Material Science: This chemical is explored for its role in developing advanced materials, including conductive polymers and nanocomposites, which have applications in energy storage and conversion.

Citations