1-(5-bromo-3,4-dihydro-2(1H)-isoquinolinyl)-2,2,2-trifluoro- Ethanone
- Product Code: 39473
CAS:
215794-11-9
| Molecular Weight: | 308.09 g./mol | Molecular Formula: | C₁₁H₉BrF₃NO |
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| Melting Point: | Boiling Point: | 403.9±45.0℃(Predicted) | |
| Density: | 1.611±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a bromo-substituted isoquinoline moiety and a trifluoroacetyl group, makes it valuable for developing potential therapeutic agents. It is often employed in the design and preparation of compounds targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. Additionally, its unique chemical properties facilitate its use in the creation of novel inhibitors for enzymes or receptors implicated in diseases such as cancer, inflammation, or infectious conditions. Researchers also leverage its reactivity in organic synthesis to construct complex heterocyclic frameworks, which are essential in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿9,000.00 |
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1-(5-bromo-3,4-dihydro-2(1H)-isoquinolinyl)-2,2,2-trifluoro- Ethanone
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a bromo-substituted isoquinoline moiety and a trifluoroacetyl group, makes it valuable for developing potential therapeutic agents. It is often employed in the design and preparation of compounds targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. Additionally, its unique chemical properties facilitate its use in the creation of novel inhibitors for enzymes or receptors implicated in diseases such as cancer, inflammation, or infectious conditions. Researchers also leverage its reactivity in organic synthesis to construct complex heterocyclic frameworks, which are essential in drug discovery and development.
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