4-Methyl-7-nitro-1H-indole
97%
- Product Code: 210028
CAS:
289483-80-3
| Molecular Weight: | 176.17 g./mol | Molecular Formula: | C₉H₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07780760 | |
| Melting Point: | Boiling Point: | 384.4°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, inflatable, light-proof |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of biologically active molecules. Its structure supports the construction of nitrogen-containing heterocyclic systems, which are common in drugs targeting neurological and inflammatory conditions. It is also employed in research settings for the preparation of fluorescent probes and sensors due to its favorable electronic properties. In medicinal chemistry, derivatives built from this scaffold are explored for their potential anticonvulsant, antidepressant, and antimicrobial activities. Its nitro group allows for further functionalization, enabling the creation of a wide range of indole-based compounds for drug discovery and materials science.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿4,170.00 |
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| 250mg | 10-20 days | ฿7,710.00 |
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| 1g | 10-20 days | ฿26,750.00 |
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4-Methyl-7-nitro-1H-indole
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of biologically active molecules. Its structure supports the construction of nitrogen-containing heterocyclic systems, which are common in drugs targeting neurological and inflammatory conditions. It is also employed in research settings for the preparation of fluorescent probes and sensors due to its favorable electronic properties. In medicinal chemistry, derivatives built from this scaffold are explored for their potential anticonvulsant, antidepressant, and antimicrobial activities. Its nitro group allows for further functionalization, enabling the creation of a wide range of indole-based compounds for drug discovery and materials science.
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