6-Bromoquinoxaline
96%
- Product Code: 120691
CAS:
50998-17-9
| Molecular Weight: | 209.04 g./mol | Molecular Formula: | C₈H₅BrN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00837757 | |
| Melting Point: | 54 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
6-Bromoquinoxaline is primarily utilized in the field of organic synthesis as a versatile building block for the creation of more complex chemical structures. Its bromine atom makes it highly reactive in various coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of quinoxaline derivatives, which are known for their biological activities, including antimicrobial, anticancer, and antiviral properties. Researchers also employ it in the design of organic electronic materials, where quinoxaline derivatives contribute to the development of light-emitting diodes (LEDs) and organic photovoltaics. Its role in these applications highlights its importance in advancing both medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 96 |
| Purity (Titration With AgNO3) | 95.5-104.5 |
| Appearance | White To Brown Powder, Fibers Or Crystals |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿530.00 |
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| 5.000 | 10-20 days | ฿2,450.00 |
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| 25.000 | 10-20 days | ฿9,980.00 |
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6-Bromoquinoxaline
6-Bromoquinoxaline is primarily utilized in the field of organic synthesis as a versatile building block for the creation of more complex chemical structures. Its bromine atom makes it highly reactive in various coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of quinoxaline derivatives, which are known for their biological activities, including antimicrobial, anticancer, and antiviral properties. Researchers also employ it in the design of organic electronic materials, where quinoxaline derivatives contribute to the development of light-emitting diodes (LEDs) and organic photovoltaics. Its role in these applications highlights its importance in advancing both medicinal chemistry and material science.
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