2-Bromo-1-(3-bromo-4-methylphenyl)ethanone

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Reagent Code: #141217
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CAS Number 60208-05-1

science Other reagents with same CAS 60208-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.97 g/mol
Formula C₉H₈Br₂O
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MDL Number MFCD19345958
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization in organic reactions, particularly in the formation of heterocyclic compounds. Commonly employed in cross-coupling reactions due to the presence of bromine atoms, which serve as sites for palladium-catalyzed reactions such as Suzuki or Heck couplings. Also utilized in the preparation of bioactive molecules where the bromo-ketone functionality enables the introduction of amine or thiol groups through nucleophilic substitution. Its reactivity makes it valuable in research laboratories for developing new drug candidates and functional materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,820.00
inventory 1g
10-20 days ฿7,600.00
inventory 5g
10-20 days ฿24,870.00

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2-Bromo-1-(3-bromo-4-methylphenyl)ethanone
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization in organic reactions, particularly in the formation of heterocyclic compounds. Commonly employed in cross-coupling reactions due to the presence of bromine atoms, which serve as sites for palladium-catalyzed reactions such as Suzuki or Heck couplings. Also utilized in the preparation of bioactive molecules where the bromo-ketone functionality enables the introduction of ami

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization in organic reactions, particularly in the formation of heterocyclic compounds. Commonly employed in cross-coupling reactions due to the presence of bromine atoms, which serve as sites for palladium-catalyzed reactions such as Suzuki or Heck couplings. Also utilized in the preparation of bioactive molecules where the bromo-ketone functionality enables the introduction of amine or thiol groups through nucleophilic substitution. Its reactivity makes it valuable in research laboratories for developing new drug candidates and functional materials.

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