5-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one
95%
- Product Code: 48932
CAS:
1100509-38-3
| Molecular Weight: | 240.0965 g./mol | Molecular Formula: | C₁₀H₁₀BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20482681 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structural framework is particularly valuable in the creation of compounds targeting neurological disorders, owing to its potential interactions with specific receptors in the brain. Additionally, it plays a role in the development of novel therapeutic agents for conditions such as anxiety, depression, and chronic pain. In organic chemistry, it is employed in the construction of complex heterocyclic structures, which are essential in drug discovery programs. Its bromine substituent also makes it a useful precursor for further functionalization through cross-coupling reactions, enabling the synthesis of diverse chemical libraries for screening purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,690.00 |
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5-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structural framework is particularly valuable in the creation of compounds targeting neurological disorders, owing to its potential interactions with specific receptors in the brain. Additionally, it plays a role in the development of novel therapeutic agents for conditions such as anxiety, depression, and chronic pain. In organic chemistry, it is employed in the construction of complex heterocyclic structures, which are essential in drug discovery programs. Its bromine substituent also makes it a useful precursor for further functionalization through cross-coupling reactions, enabling the synthesis of diverse chemical libraries for screening purposes.
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