Place of Origin: | China |
Brand Name: | China |
Minimum Order Quantity: | Depens |
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Delivery Time: | 15 working days |
CAS: | 161957-61-5 | MF: | C8H6BrFO |
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Boiling Point: | 252.4±25.0 °C(Predicted) | Density: | 1.535±0.06 G/cm3(Predicted) |
Steam Pressure: | 0.1 ± 0.4 MmHg At 25 ° C | Molecular Weight: | 217.04 |
Appearance: | Solid | ||
Highlight: | CAS 58534-95-9 Organic Synthesis Intermediates,C6H5BrFN Organic Synthesis Intermediates,Organic Synthesis Intermediates Catalyst |
Organic Synthesis Intermediates C6H5BrFN Catalyst CAS 58534-95-9
Features
3-Bromo-2-fluoroacetophenone is an organic compound with the chemical formula C8H6BrFO. It is an ethanone derivative containing both bromine and fluorine atoms on the benzene ring.
3-Bromo-2-fluoroacetophenone is widely used in organic synthesis. It can be used as the starting material or intermediate of Organic reaction to participate in esterification, functionalization of carbonyl compounds and other reactions. Due to its unique structure and chemical properties, it plays an important role in the preparation of compounds such as drugs, pesticides, and fragrances.
When using 3-bromo-2-fluoroacetophenone for experiments or synthesis, it is necessary to follow the safety operation procedures. Use appropriate protective equipment and operate in accordance with relevant laws and regulations. If it needs to be applied in the fields of medicine and pesticides, it is recommended to seek professional guidance and consultation to ensure the safety and legality of the operation.
Specification
product Name | 3'-Bromo-2'-Fluoroacetophenone |
Density | 1.535±0.06 g/cm3(Predicted) |
Molecular Formula | C8H6BrFO |
Molecular Weight | 217.04 |
Appearance | Solid |
Boiling point | 252.4±25.0 °C(Predicted) |
Mol | 161957-61-5.mol |
Storage conditions: | 2-8°C |
Applications
3-Bromo-2-fluoroacetophenone is widely used in drug synthesis, pesticide synthesis, chemical research and other fields, providing powerful tools for scientists and researchers to explore new chemical reactions and synthesis methods, and develop compounds with specific activities and biological activities.
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