1-[(4R)-4,5-Dihydro-4-isopropyl-2-oxazolyl]isoquinoline
≥98%,99%e.e.
- Product Code: 70594
CAS:
280755-83-1
| Molecular Weight: | 240.3 g./mol | Molecular Formula: | C₁₅H₁₆N₂O |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 407.1±18.0 °C | |
| Density: | 1.18±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block for the synthesis of more complex molecules. Its structure, featuring an oxazoline ring fused with an isoquinoline moiety, makes it valuable for developing pharmaceuticals, particularly those targeting neurological disorders or acting as enzyme inhibitors. Researchers often explore its potential in designing drugs that interact with specific biological pathways, leveraging its unique chemical framework to enhance binding affinity and selectivity. Additionally, it may be employed in asymmetric synthesis due to its chiral center, contributing to the production of enantiomerically pure compounds. Its applications are largely experimental, focusing on drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,097.00 |
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| 0.250 | 10-20 days | ฿5,004.00 |
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1-[(4R)-4,5-Dihydro-4-isopropyl-2-oxazolyl]isoquinoline
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block for the synthesis of more complex molecules. Its structure, featuring an oxazoline ring fused with an isoquinoline moiety, makes it valuable for developing pharmaceuticals, particularly those targeting neurological disorders or acting as enzyme inhibitors. Researchers often explore its potential in designing drugs that interact with specific biological pathways, leveraging its unique chemical framework to enhance binding affinity and selectivity. Additionally, it may be employed in asymmetric synthesis due to its chiral center, contributing to the production of enantiomerically pure compounds. Its applications are largely experimental, focusing on drug discovery and development processes.
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