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Catalog Number:
44967
CAS Number:
10486-61-0
3-Iodothiophene
Purity:
≥ 98% (GC)
Synonym(s):
3-Thienyl iodide
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Product Information

3-Iodothiophene is a versatile organosulfur compound that plays a significant role in various chemical applications, particularly in the fields of organic synthesis and materials science. This compound is recognized for its unique properties, including its ability to participate in cross-coupling reactions, making it a valuable building block for the synthesis of complex organic molecules. Researchers and industry professionals utilize 3-Iodothiophene in the development of functionalized thiophene derivatives, which are essential in the production of organic semiconductors, photovoltaic devices, and advanced materials. Its iodine substituent enhances its reactivity, allowing for efficient transformations that are crucial in the design of novel compounds with tailored properties.

In addition to its synthetic utility, 3-Iodothiophene is also explored for its potential applications in medicinal chemistry, particularly in the development of new pharmaceuticals. Its unique structure and reactivity can lead to the discovery of compounds with enhanced biological activity. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, making it an ideal choice for researchers looking to innovate in organic synthesis and materials development.

Synonyms
3-Thienyl iodide
CAS Number
10486-61-0
Purity
≥ 98% (GC)
Molecular Formula
C4H3IS
Molecular Weight
210.03
MDL Number
MFCD00037901
PubChem ID
66332
Melting Point
-13 °C
Density
2.06
Appearance
Colorless to yellow clear liquid
Boiling Point
75 °C/14 mmHg
Refractive Index
n20D 1.65
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Thienyl iodide
CAS Number
10486-61-0
Purity
≥ 98% (GC)
Molecular Formula
C4H3IS
Molecular Weight
210.03
MDL Number
MFCD00037901
PubChem ID
66332
Melting Point
-13 °C
Density
2.06
Appearance
Colorless to yellow clear liquid
Boiling Point
75 °C/14 mmHg
Refractive Index
n20D 1.65
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Iodothiophene is widely utilized in research focused on:

  • Organic Electronics: This compound is a key building block in the synthesis of organic semiconductors, which are essential for developing flexible and lightweight electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells.
  • Pharmaceutical Development: It serves as an intermediate in the synthesis of various pharmaceuticals, particularly those targeting specific biological pathways, enhancing the efficiency of drug discovery processes.
  • Material Science: Used in the fabrication of conductive polymers, 3-iodothiophene contributes to the development of advanced materials with applications in sensors and energy storage devices, offering improved performance compared to traditional materials.
  • Agrochemicals: This compound is involved in the production of agrochemical products, including pesticides and herbicides, helping to improve crop yields and pest resistance in agriculture.
  • Research in Catalysis: It plays a role in catalysis research, particularly in the development of new catalytic systems that can facilitate chemical reactions more efficiently, leading to greener and more sustainable chemical processes.

Citations