3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
≥97%(GC)
- Product Code: 68139
CAS:
850881-09-3
| Molecular Weight: | 294.26 g./mol | Molecular Formula: | C₁₆H₂₇BO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11045447 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.99 | Storage Condition: | Room temperature, dry, inert gas storage |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the field of polymer chemistry. It serves as a key intermediate in the production of conjugated polymers, which are essential for creating organic electronic materials. These materials are widely applied in the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The boronate ester group in the compound facilitates cross-coupling reactions, such as Suzuki-Miyaura reactions, enabling the construction of complex organic molecules with high precision. Its thiophene moiety contributes to the electronic properties of the resulting polymers, enhancing their conductivity and stability. This makes it a valuable component in the design of advanced materials for next-generation electronic devices.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Light yellow clear liquid |
| PURITYGC | 97 100% |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,860.00 |
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| 1.000 | 10-20 days | ฿5,580.00 |
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3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
This chemical is primarily used in organic synthesis, particularly in the field of polymer chemistry. It serves as a key intermediate in the production of conjugated polymers, which are essential for creating organic electronic materials. These materials are widely applied in the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The boronate ester group in the compound facilitates cross-coupling reactions, such as Suzuki-Miyaura reactions, enabling the construction of complex organic molecules with high precision. Its thiophene moiety contributes to the electronic properties of the resulting polymers, enhancing their conductivity and stability. This makes it a valuable component in the design of advanced materials for next-generation electronic devices.
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