1-[(4S)-4,5-Dihydro-4-isopropyl-2-oxazolyl]isoquinoline
≥98%,99%e.e.
- Product Code: 70598
CAS:
1701405-00-6
| 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 in the synthesis of more complex molecules. Its structure, featuring an isoquinoline moiety and an oxazoline ring, makes it valuable for developing potential pharmaceutical agents. Researchers often employ it in the design of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its stereochemistry and functional groups allow for precise interactions with biological targets, making it a candidate for drug discovery efforts, particularly in areas like anti-inflammatory, anticancer, or neurological therapies. Additionally, it may be explored in asymmetric synthesis due to its chiral center, contributing to the production of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿1,071.00 |
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| 0.100 | 10-20 days | ฿2,070.00 |
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| 0.250 | 10-20 days | ฿4,905.00 |
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| 1.000 | 10-20 days | ฿19,557.00 |
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1-[(4S)-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 in the synthesis of more complex molecules. Its structure, featuring an isoquinoline moiety and an oxazoline ring, makes it valuable for developing potential pharmaceutical agents. Researchers often employ it in the design of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its stereochemistry and functional groups allow for precise interactions with biological targets, making it a candidate for drug discovery efforts, particularly in areas like anti-inflammatory, anticancer, or neurological therapies. Additionally, it may be explored in asymmetric synthesis due to its chiral center, contributing to the production of enantiomerically pure substances.
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