4,6-Difluoro-1H-indole-2,3-dione
97%
- Product Code: 45919
CAS:
126674-93-9
| Molecular Weight: | 183.12 g./mol | Molecular Formula: | C₈H₃F₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03618552 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
4,6-Difluoro-1H-indole-2,3-dione is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting neurological and psychiatric disorders. Its structure is often incorporated into molecules designed to interact with specific enzymes or receptors in the brain, making it valuable in the creation of potential therapeutic agents. Additionally, it is used in the synthesis of fluorescent dyes and probes for biochemical assays, aiding in the study of cellular processes and molecular interactions. Its unique fluorinated indole core also contributes to the development of agrochemicals, where it may be used to create compounds with pesticidal or herbicidal properties.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| APPEARANCE | YELLOW TO BROWN OR RED crystal powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿860.00 |
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| 5.000 | 10-20 days | ฿2,520.00 |
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| 25.000 | 10-20 days | ฿6,200.00 |
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4,6-Difluoro-1H-indole-2,3-dione
4,6-Difluoro-1H-indole-2,3-dione is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting neurological and psychiatric disorders. Its structure is often incorporated into molecules designed to interact with specific enzymes or receptors in the brain, making it valuable in the creation of potential therapeutic agents. Additionally, it is used in the synthesis of fluorescent dyes and probes for biochemical assays, aiding in the study of cellular processes and molecular interactions. Its unique fluorinated indole core also contributes to the development of agrochemicals, where it may be used to create compounds with pesticidal or herbicidal properties.
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