2-(3-Iodopropyl)thiophene
97%
- Product Code: 41532
CAS:
854625-59-5
| Molecular Weight: | 252.12 g./mol | Molecular Formula: | C₇H₉IS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27930039 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules for pharmaceuticals and materials science. It serves as a key intermediate in the preparation of thiophene-based compounds, which are valuable in the creation of conductive polymers and organic semiconductors. These materials are essential in the production of electronic devices such as organic light-emitting diodes (OLEDs) and solar cells. Additionally, it is employed in medicinal chemistry for the synthesis of potential drug candidates, where the thiophene moiety can impart specific biological activity. Its iodine atom also makes it a useful building block for further functionalization through cross-coupling reactions, enabling the construction of diverse molecular architectures.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to yellow liquid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,360.00 |
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| 0.250 | 10-20 days | ฿5,060.00 |
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| 1.000 | 10-20 days | ฿15,180.00 |
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2-(3-Iodopropyl)thiophene
This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules for pharmaceuticals and materials science. It serves as a key intermediate in the preparation of thiophene-based compounds, which are valuable in the creation of conductive polymers and organic semiconductors. These materials are essential in the production of electronic devices such as organic light-emitting diodes (OLEDs) and solar cells. Additionally, it is employed in medicinal chemistry for the synthesis of potential drug candidates, where the thiophene moiety can impart specific biological activity. Its iodine atom also makes it a useful building block for further functionalization through cross-coupling reactions, enabling the construction of diverse molecular architectures.
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