Racemic-(3R,3aR,7aR)-tert-butyl 3-(aminomethyl)hexahydrofuro[3,4-c]pyridine-5(3H)-carboxylate
95%
- Product Code: 87086
CAS:
1350475-45-4
| Molecular Weight: | 256.35 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21362284 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of complex pharmaceutical agents. Its structure, featuring a fused furo[3,4-c]pyridine ring system, makes it valuable for the development of drugs targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. The presence of the aminomethyl group allows for further functionalization, enabling the creation of derivatives with potential therapeutic activity. Additionally, the tert-butyl ester group provides stability and facilitates purification during synthetic processes. Its application is often seen in the preparation of compounds with potential analgesic, anti-inflammatory, or antipsychotic properties. Researchers leverage its scaffold to explore novel bioactive molecules, particularly in the design of small-molecule inhibitors or modulators of specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿39,555.00 |
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Racemic-(3R,3aR,7aR)-tert-butyl 3-(aminomethyl)hexahydrofuro[3,4-c]pyridine-5(3H)-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of complex pharmaceutical agents. Its structure, featuring a fused furo[3,4-c]pyridine ring system, makes it valuable for the development of drugs targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. The presence of the aminomethyl group allows for further functionalization, enabling the creation of derivatives with potential therapeutic activity. Additionally, the tert-butyl ester group provides stability and facilitates purification during synthetic processes. Its application is often seen in the preparation of compounds with potential analgesic, anti-inflammatory, or antipsychotic properties. Researchers leverage its scaffold to explore novel bioactive molecules, particularly in the design of small-molecule inhibitors or modulators of specific biological targets.
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