5-Bromo-1H-inden-2(3H)-one
97%
- Product Code: 120143
CAS:
174349-93-0
| Molecular Weight: | 211.06 g./mol | Molecular Formula: | C₉H₇BrO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07778391 | |
| Melting Point: | Boiling Point: | 353.8°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
5-Bromo-1H-inden-2(3H)-one is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure is particularly valuable in the construction of indene-based molecules, which are often explored for their potential biological activities. Researchers employ this compound in the synthesis of novel drug candidates targeting conditions such as inflammation, cancer, and central nervous system disorders. Additionally, it serves as a building block in the preparation of complex organic frameworks, enabling the study of structure-activity relationships in medicinal chemistry. Its bromine substituent also makes it a versatile reagent for further functionalization through cross-coupling reactions, enhancing its utility in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,728.00 |
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| 0.250 | 10-20 days | ฿2,835.00 |
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| 1.000 | 10-20 days | ฿7,209.00 |
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| 5.000 | 10-20 days | ฿23,607.00 |
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5-Bromo-1H-inden-2(3H)-one
5-Bromo-1H-inden-2(3H)-one is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure is particularly valuable in the construction of indene-based molecules, which are often explored for their potential biological activities. Researchers employ this compound in the synthesis of novel drug candidates targeting conditions such as inflammation, cancer, and central nervous system disorders. Additionally, it serves as a building block in the preparation of complex organic frameworks, enabling the study of structure-activity relationships in medicinal chemistry. Its bromine substituent also makes it a versatile reagent for further functionalization through cross-coupling reactions, enhancing its utility in drug discovery and development processes.
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