5-Methoxy-1H-indole-3-carbonitrile
95%
- Product Code: 81484
CAS:
23084-36-8
| Molecular Weight: | 172.18 g./mol | Molecular Formula: | C₁₀H₈N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06654845 | |
| Melting Point: | Boiling Point: | 385 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a crucial intermediate for the development of more complex molecules. Its structure, featuring both methoxy and nitrile functional groups, makes it a versatile building block in the synthesis of various heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, antifungal, and anticancer properties. Additionally, it is employed in the pharmaceutical industry for the research and development of new drugs, particularly those targeting neurological disorders, due to its indole core which is a common motif in many bioactive molecules. Researchers also leverage its reactivity in the creation of novel materials with specific electronic or photonic properties, contributing to advancements in material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,071.00 |
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| 0.250 | 10-20 days | ฿1,791.00 |
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| 1.000 | 10-20 days | ฿4,491.00 |
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5-Methoxy-1H-indole-3-carbonitrile
This compound is primarily utilized in the field of organic synthesis, where it serves as a crucial intermediate for the development of more complex molecules. Its structure, featuring both methoxy and nitrile functional groups, makes it a versatile building block in the synthesis of various heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, antifungal, and anticancer properties. Additionally, it is employed in the pharmaceutical industry for the research and development of new drugs, particularly those targeting neurological disorders, due to its indole core which is a common motif in many bioactive molecules. Researchers also leverage its reactivity in the creation of novel materials with specific electronic or photonic properties, contributing to advancements in material science.
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