tert-Butyl 3-(2-cyanopropan-2-yl)-1H-indole-1-carboxylate
98%
- Product Code: 117391
CAS:
380626-46-0
| Molecular Weight: | 284.35 g./mol | Molecular Formula: | C₁₇H₂₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02323443 | |
| Melting Point: | Boiling Point: | 422.1 °C at 760 mmHg | |
| Density: | 1.06 g/cm3 | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of complex molecules, especially those containing indole structures, which are prevalent in many biologically active compounds. Its application is significant in the production of potential drug candidates, where the indole moiety plays a crucial role in binding to biological targets. Additionally, it is used in research settings to explore novel chemical reactions and pathways, aiding in the discovery of new therapeutic agents. The presence of the cyano and tert-butyl groups enhances its reactivity, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,278.00 |
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| 0.250 | 10-20 days | ฿17,460.00 |
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| 1.000 | 10-20 days | ฿47,133.00 |
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tert-Butyl 3-(2-cyanopropan-2-yl)-1H-indole-1-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of complex molecules, especially those containing indole structures, which are prevalent in many biologically active compounds. Its application is significant in the production of potential drug candidates, where the indole moiety plays a crucial role in binding to biological targets. Additionally, it is used in research settings to explore novel chemical reactions and pathways, aiding in the discovery of new therapeutic agents. The presence of the cyano and tert-butyl groups enhances its reactivity, making it a versatile building block in medicinal chemistry.
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