2-Bromo-1-(5-chloro-2-methoxyphenyl)ethanone
≥95%
- Product Code: 85932
CAS:
111841-05-5
Molecular Weight: | 263.52 g./mol | Molecular Formula: | C₉H₈BrClO₂ |
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EC Number: | MDL Number: | MFCD01793848 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
2-Bromo-1-(5-chloro-2-methoxyphenyl)ethanone is primarily used in organic synthesis as a key intermediate for the production of various pharmaceutical compounds. Its reactive bromo and carbonyl groups make it a valuable building block in the synthesis of complex molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the preparation of agrochemicals, where it serves as a precursor for the synthesis of herbicides and insecticides. The compound’s structure allows for further functionalization, making it versatile in the creation of biologically active molecules. Researchers also utilize it in the development of novel materials and chemical probes for studying biochemical pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $53.80 |
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0.250 | 10-20 days | $90.96 |
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1.000 | 10-20 days | $244.92 |
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2-Bromo-1-(5-chloro-2-methoxyphenyl)ethanone
2-Bromo-1-(5-chloro-2-methoxyphenyl)ethanone is primarily used in organic synthesis as a key intermediate for the production of various pharmaceutical compounds. Its reactive bromo and carbonyl groups make it a valuable building block in the synthesis of complex molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the preparation of agrochemicals, where it serves as a precursor for the synthesis of herbicides and insecticides. The compound’s structure allows for further functionalization, making it versatile in the creation of biologically active molecules. Researchers also utilize it in the development of novel materials and chemical probes for studying biochemical pathways.
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