1-(1H-Indol-6-yl)cyclopropanol
97%
- Product Code: 39118
CAS:
1891321-97-3
| Molecular Weight: | 173.2111 g./mol | Molecular Formula: | C₁₁H₁₁NO |
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| EC Number: | MDL Number: | MFCD28357582 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
1-(1H-Indol-6-yl)cyclopropanol is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and psychiatric disorders. Its indole and cyclopropanol moieties make it a valuable scaffold for designing molecules that interact with serotonin receptors, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, this compound is explored in the development of potential anticancer agents due to its ability to modulate cellular pathways involved in tumor growth and apoptosis. Researchers also investigate its use in creating novel enzyme inhibitors, leveraging its structural properties to enhance binding affinity and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,527.00 |
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1-(1H-Indol-6-yl)cyclopropanol
1-(1H-Indol-6-yl)cyclopropanol is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and psychiatric disorders. Its indole and cyclopropanol moieties make it a valuable scaffold for designing molecules that interact with serotonin receptors, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, this compound is explored in the development of potential anticancer agents due to its ability to modulate cellular pathways involved in tumor growth and apoptosis. Researchers also investigate its use in creating novel enzyme inhibitors, leveraging its structural properties to enhance binding affinity and selectivity.
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