2-(5-Formylthiophen-2-yl)benzonitrile
95%
- Product Code: 41754
CAS:
194416-92-7
| Molecular Weight: | 213.26 g./mol | Molecular Formula: | C₁₂H₇NOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06740277 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the synthesis of organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a formyl group and a nitrile group, makes it a versatile intermediate in organic reactions. It is often employed in the construction of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, it serves as a building block in the production of materials with potential applications in organic electronics and optoelectronics, such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Its reactivity also allows for its use in coupling reactions, contributing to the creation of complex molecules with specific functional properties.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,872.00 |
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| 0.250 | 10-20 days | ฿19,818.00 |
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2-(5-Formylthiophen-2-yl)benzonitrile
This chemical is primarily utilized in the synthesis of organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a formyl group and a nitrile group, makes it a versatile intermediate in organic reactions. It is often employed in the construction of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, it serves as a building block in the production of materials with potential applications in organic electronics and optoelectronics, such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Its reactivity also allows for its use in coupling reactions, contributing to the creation of complex molecules with specific functional properties.
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