6-Bromo-2-ethyl-3,4-dihydroisoquinolin-1(2H)-one
98%
- Product Code: 49853
CAS:
879887-28-2
| Molecular Weight: | 254.1231 g./mol | Molecular Formula: | C₁₁H₁₂BrNO |
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| EC Number: | MDL Number: | MFCD27931282 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
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 structure is particularly valuable in the development of compounds targeting neurological disorders, such as Alzheimer's disease and other neurodegenerative conditions. Researchers leverage its bromo and carbonyl functional groups to introduce modifications that enhance binding affinity to specific biological targets, such as enzymes or receptors involved in disease pathways. Additionally, it serves as a building block in the creation of small-molecule inhibitors, which are critical in drug discovery efforts aimed at treating cancers and inflammatory diseases. Its versatility in chemical reactions makes it a valuable tool for designing and optimizing novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €78.83 |
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6-Bromo-2-ethyl-3,4-dihydroisoquinolin-1(2H)-one
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting neurological disorders, such as Alzheimer's disease and other neurodegenerative conditions. Researchers leverage its bromo and carbonyl functional groups to introduce modifications that enhance binding affinity to specific biological targets, such as enzymes or receptors involved in disease pathways. Additionally, it serves as a building block in the creation of small-molecule inhibitors, which are critical in drug discovery efforts aimed at treating cancers and inflammatory diseases. Its versatility in chemical reactions makes it a valuable tool for designing and optimizing novel therapeutic agents.
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