methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylate
99%
- Product Code: 64519
CAS:
885958-43-0
Molecular Weight: | 259.35 g./mol | Molecular Formula: | C₁₆H₂₁NO₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its unique structure, featuring a cyclopentapyrrole core, makes it valuable for developing compounds with potential therapeutic effects, particularly in the central nervous system. Researchers often employ it in the design and synthesis of novel drug candidates targeting neurological disorders, such as anxiety, depression, or neurodegenerative diseases. Additionally, its benzyl and ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. This chemical is also explored in the development of small molecule inhibitors for specific enzymes or receptors, contributing to advancements in drug discovery and development pipelines.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless oil |
PURITY | 98.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿5,530.00 |
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1.000 | 10-20 days | ฿13,380.00 |
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5.000 | 10-20 days | ฿35,000.00 |
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methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its unique structure, featuring a cyclopentapyrrole core, makes it valuable for developing compounds with potential therapeutic effects, particularly in the central nervous system. Researchers often employ it in the design and synthesis of novel drug candidates targeting neurological disorders, such as anxiety, depression, or neurodegenerative diseases. Additionally, its benzyl and ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. This chemical is also explored in the development of small molecule inhibitors for specific enzymes or receptors, contributing to advancements in drug discovery and development pipelines.
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