3-Iodocarbazole
99%
- Product Code: 94102
Alias:
3-iodo-9H-carbazole;3-iodocarbazole;3-iodocarbazole
CAS:
16807-13-9
Properties:
solid
| Molecular Weight: | 293.11 g./mol | Molecular Formula: | C₁₂H₈IN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00267746 | |
| Melting Point: | 195-197℃ | Boiling Point: | |
| Density: | 1.854g/cm3 | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. It is particularly valuable in the development of carbazole-based compounds, which exhibit significant biological activity, including antitumor, antimicrobial, and anti-inflammatory properties. Additionally, it plays a role in the creation of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to enhance charge transport properties. Its iodine atom makes it a useful building block for further functionalization through cross-coupling reactions, enabling the construction of complex molecular architectures.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98.5 100% |
| Melting point | 197 201? |
| Appearance | White to off-white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿640.00 |
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| 25.000 | 10-20 days | ฿2,780.00 |
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3-Iodocarbazole
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. It is particularly valuable in the development of carbazole-based compounds, which exhibit significant biological activity, including antitumor, antimicrobial, and anti-inflammatory properties. Additionally, it plays a role in the creation of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to enhance charge transport properties. Its iodine atom makes it a useful building block for further functionalization through cross-coupling reactions, enabling the construction of complex molecular architectures.
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