6-Bromo-4-(trifluoromethyl)-2,3-dihydro-1H-inden-1-one
97%
- Product Code: 49916
CAS:
1273655-84-7
| Molecular Weight: | 279.0533 g./mol | Molecular Formula: | C₁₀H₆BrF₃O |
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| EC Number: | MDL Number: | MFCD18647940 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring both a bromo and trifluoromethyl group, makes it valuable for introducing these functional groups into target compounds. In drug discovery, it serves as a building block for developing potential therapeutic agents, especially in the synthesis of biologically active molecules targeting specific enzymes or receptors. Additionally, it finds application in materials science, where it can be used to create specialized polymers or coatings with enhanced properties due to the presence of the trifluoromethyl group, which often imparts chemical stability and hydrophobicity. Its reactivity also allows for further derivatization, enabling the creation of diverse chemical libraries for screening and research purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,211.00 |
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6-Bromo-4-(trifluoromethyl)-2,3-dihydro-1H-inden-1-one
This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring both a bromo and trifluoromethyl group, makes it valuable for introducing these functional groups into target compounds. In drug discovery, it serves as a building block for developing potential therapeutic agents, especially in the synthesis of biologically active molecules targeting specific enzymes or receptors. Additionally, it finds application in materials science, where it can be used to create specialized polymers or coatings with enhanced properties due to the presence of the trifluoromethyl group, which often imparts chemical stability and hydrophobicity. Its reactivity also allows for further derivatization, enabling the creation of diverse chemical libraries for screening and research purposes.
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