5-Fluoro-2-methylindole
97%
- Product Code: 119872
CAS:
399-72-4
| Molecular Weight: | 149.16 g./mol | Molecular Formula: | C₉H₈FN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02093649 | |
| Melting Point: | 98-101 °C(lit.) | Boiling Point: | 112-120C |
| Density: | Storage Condition: | room temperature |
Product Description:
5-Fluoro-2-methylindole is primarily used in the synthesis of various pharmaceutical compounds. It serves as a key intermediate in the development of drugs targeting neurological disorders, particularly those involving serotonin receptors. Its structural properties make it valuable in creating molecules that can modulate serotonin pathways, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, it is utilized in organic chemistry research for the preparation of indole derivatives, which are explored for their potential biological activities, including anticancer and anti-inflammatory properties. Its application extends to agrochemical research, where it is employed in the development of novel pesticides and herbicides.
Product Specification:
| Test | Specification |
|---|---|
| Carbon | 69.9-75 |
| Nitrogen | 9-9.7 |
| Purity (GC) | 97-100 |
| Appearance | Yellow To Brown Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿700.00 |
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| 5.000 | 10-20 days | ฿2,480.00 |
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| 25.000 | 10-20 days | ฿9,770.00 |
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5-Fluoro-2-methylindole
5-Fluoro-2-methylindole is primarily used in the synthesis of various pharmaceutical compounds. It serves as a key intermediate in the development of drugs targeting neurological disorders, particularly those involving serotonin receptors. Its structural properties make it valuable in creating molecules that can modulate serotonin pathways, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, it is utilized in organic chemistry research for the preparation of indole derivatives, which are explored for their potential biological activities, including anticancer and anti-inflammatory properties. Its application extends to agrochemical research, where it is employed in the development of novel pesticides and herbicides.
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