1-Bromo-3-(difluoromethoxy)-5-nitrobenzene

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Reagent Code: #40014
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CAS Number 1261441-47-7

science Other reagents with same CAS 1261441-47-7

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Weight 268.0100 g/mol
Formula C₇H₄BrF₂NO₃
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MDL Number MFCD18390953
inventory_2 Storage & Handling
Storage room temperature

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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex molecules. Its unique structure, featuring bromine, difluoromethoxy, and nitro groups, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic functionalities into target molecules. Additionally, its nitro group can be reduced to an amine, opening pathways for further functionalization. Researchers also explore its potential in material science, particularly in the synthesis of advanced polymers and coatings with specific electronic or optical properties. Its fluorine-containing moiety can enhance the stability and bioavailability of drug candidates, making it a key component in medicinal chemistry.

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inventory 1g
10-20 days ฿5,553.00

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1-Bromo-3-(difluoromethoxy)-5-nitrobenzene
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex molecules. Its unique structure, featuring bromine, difluoromethoxy, and nitro groups, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic functionalities into target molecules. Additionally, it

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex molecules. Its unique structure, featuring bromine, difluoromethoxy, and nitro groups, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic functionalities into target molecules. Additionally, its nitro group can be reduced to an amine, opening pathways for further functionalization. Researchers also explore its potential in material science, particularly in the synthesis of advanced polymers and coatings with specific electronic or optical properties. Its fluorine-containing moiety can enhance the stability and bioavailability of drug candidates, making it a key component in medicinal chemistry.

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