tert-Butyl 6-fluoro-3-(hydroxymethyl)-1H-indole-1-carboxylate
95%
- Product Code: 85549
CAS:
1260801-80-6
| Molecular Weight: | 265.28 g./mol | Molecular Formula: | C₁₄H₁₆FNO₃ |
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| EC Number: | MDL Number: | MFCD16037107 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic compounds. It serves as a key intermediate in the production of biologically active molecules, often targeting therapeutic areas such as oncology and neurology. Its indole core structure is valuable for designing compounds that interact with specific enzymes or receptors in the body. Additionally, the presence of functional groups like the fluoro and hydroxymethyl substituents allows for further chemical modifications, enabling the creation of diverse derivatives with potential medicinal applications. Researchers also leverage its stability and reactivity in multi-step synthetic processes to develop novel drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft72,046.46 |
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| 0.250 | 10-20 days | Ft131,099.35 |
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tert-Butyl 6-fluoro-3-(hydroxymethyl)-1H-indole-1-carboxylate
This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic compounds. It serves as a key intermediate in the production of biologically active molecules, often targeting therapeutic areas such as oncology and neurology. Its indole core structure is valuable for designing compounds that interact with specific enzymes or receptors in the body. Additionally, the presence of functional groups like the fluoro and hydroxymethyl substituents allows for further chemical modifications, enabling the creation of diverse derivatives with potential medicinal applications. Researchers also leverage its stability and reactivity in multi-step synthetic processes to develop novel drug candidates.
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