1,5-Dibromo-3-fluoro-2-methoxybenzene

97%

Reagent Code: #39029
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CAS Number 202982-75-0

science Other reagents with same CAS 202982-75-0

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Weight 283.9204 g/mol
Formula C₇H₅Br₂FO
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for the production of more complex chemical compounds. Its structure, featuring bromine and fluorine substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the methoxy group enhances its reactivity in electrophilic substitution reactions, allowing for further functionalization. It is also employed in the synthesis of liquid crystals and organic electronic materials due to its ability to modify electronic properties. Its halogenated aromatic structure is beneficial in creating compounds with specific biological activities, making it relevant in medicinal chemistry research.

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inventory 100mg
10-20 days ฿4,734.00

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1,5-Dibromo-3-fluoro-2-methoxybenzene
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for the production of more complex chemical compounds. Its structure, featuring bromine and fluorine substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the methoxy group enhances its reactivity in electrophilic substitution reactions, allowing

This chemical is primarily utilized in organic synthesis as a versatile intermediate for the production of more complex chemical compounds. Its structure, featuring bromine and fluorine substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the methoxy group enhances its reactivity in electrophilic substitution reactions, allowing for further functionalization. It is also employed in the synthesis of liquid crystals and organic electronic materials due to its ability to modify electronic properties. Its halogenated aromatic structure is beneficial in creating compounds with specific biological activities, making it relevant in medicinal chemistry research.

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