1-(Bromomethyl)-2-fluoro-3-methoxybenzene
98%
- Product Code: 39638
CAS:
447463-56-1
Molecular Weight: | 219.0500 g./mol | Molecular Formula: | C₈H₈BrFO |
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EC Number: | MDL Number: | MFCD09743597 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. The presence of bromomethyl and fluoro groups makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are crucial for creating carbon-carbon or carbon-nitrogen bonds. Additionally, its methoxy group can be further modified or deprotected to introduce additional functional groups, enhancing its utility in medicinal chemistry. It is also used in agrochemical research for the synthesis of novel pesticides or herbicides, where its structural features contribute to the bioactivity of the final product.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | £13.23 |
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1-(Bromomethyl)-2-fluoro-3-methoxybenzene
This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. The presence of bromomethyl and fluoro groups makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are crucial for creating carbon-carbon or carbon-nitrogen bonds. Additionally, its methoxy group can be further modified or deprotected to introduce additional functional groups, enhancing its utility in medicinal chemistry. It is also used in agrochemical research for the synthesis of novel pesticides or herbicides, where its structural features contribute to the bioactivity of the final product.
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