4-(1H-Pyrrolo[2,3-d]pyrimidin-4-yl)morpholine
95%
- Product Code: 46097
CAS:
90870-83-0
| Molecular Weight: | 204.2285 g./mol | Molecular Formula: | C₁₀H₁₂N₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18904308 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound 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 molecules, particularly those targeting kinase enzymes. Its structure is often incorporated into inhibitors that are designed to treat cancers and inflammatory diseases. Researchers leverage its pyrrolopyrimidine core to enhance binding affinity and selectivity towards specific protein targets, making it valuable in the design of therapeutic agents. Additionally, it is explored in the development of compounds for neurological disorders due to its potential to modulate signaling pathways in the brain. Its versatility in chemical modifications allows for the creation of diverse derivatives with tailored pharmacological properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft41,307.93 |
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4-(1H-Pyrrolo[2,3-d]pyrimidin-4-yl)morpholine
This compound 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 molecules, particularly those targeting kinase enzymes. Its structure is often incorporated into inhibitors that are designed to treat cancers and inflammatory diseases. Researchers leverage its pyrrolopyrimidine core to enhance binding affinity and selectivity towards specific protein targets, making it valuable in the design of therapeutic agents. Additionally, it is explored in the development of compounds for neurological disorders due to its potential to modulate signaling pathways in the brain. Its versatility in chemical modifications allows for the creation of diverse derivatives with tailored pharmacological properties.
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