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

97%

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
badge Registry Numbers
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.

Available Sizes & Pricing

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