Methyl 1,4,5,6,7,8-hexahydrocyclohepta[b]pyrrole-2-carboxylate
97%
- Product Code: 38977
CAS:
100445-46-3
| Molecular Weight: | 193.2400 g./mol | Molecular Formula: | C₁₁H₁₅NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21337186 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique cyclohepta[b]pyrrole framework makes it valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers employ it in the preparation of analogs that can be screened for biological activity, particularly in drug discovery projects targeting neurological or anti-inflammatory pathways. Additionally, it serves as a building block in the creation of novel materials with specific electronic or optical properties, contributing to advancements in material science. Its ester functional group also allows for further chemical modifications, making it versatile in various synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,929.00 |
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Methyl 1,4,5,6,7,8-hexahydrocyclohepta[b]pyrrole-2-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique cyclohepta[b]pyrrole framework makes it valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers employ it in the preparation of analogs that can be screened for biological activity, particularly in drug discovery projects targeting neurological or anti-inflammatory pathways. Additionally, it serves as a building block in the creation of novel materials with specific electronic or optical properties, contributing to advancements in material science. Its ester functional group also allows for further chemical modifications, making it versatile in various synthetic routes.
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