2'-Bromo-4'-fluoroacetophenone
98%
- Product Code: 143582
CAS:
1006-39-9
| Molecular Weight: | 217.04 g./mol | Molecular Formula: | C₈HC₆BrFO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00077464 | |
| Melting Point: | 48-50°C | Boiling Point: | 150°C 12mm |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring fluorinated aromatic ketone structures. Its reactivity allows for further functionalization in multi-step organic reactions, especially in the formation of carbon-carbon bonds via nucleophilic substitution or cross-coupling reactions. Commonly employed in the production of anti-inflammatory and analgesic agents due to the presence of both bromo and fluoro substituents that influence biological activity. Also utilized in agrochemical synthesis for creating herbicides and fungicides where halogenated acetophenone derivatives enhance target specificity and stability. Suitable for research applications in medicinal chemistry for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿320.00 |
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| 5g | 10-20 days | ฿1,100.00 |
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| 25g | 10-20 days | ฿5,340.00 |
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| 100g | 10-20 days | ฿18,380.00 |
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2'-Bromo-4'-fluoroacetophenone
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring fluorinated aromatic ketone structures. Its reactivity allows for further functionalization in multi-step organic reactions, especially in the formation of carbon-carbon bonds via nucleophilic substitution or cross-coupling reactions. Commonly employed in the production of anti-inflammatory and analgesic agents due to the presence of both bromo and fluoro substituents that influence biological activity. Also utilized in agrochemical synthesis for creating herbicides and fungicides where halogenated acetophenone derivatives enhance target specificity and stability. Suitable for research applications in medicinal chemistry for structure-activity relationship (SAR) studies.
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