(3-Bromo-2-iodophenyl)methanol

97%

Reagent Code: #155237
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CAS Number 1261571-03-2

science Other reagents with same CAS 1261571-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.93 g/mol
Formula C₇H₆BrIO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its functional groups—bromine and iodine—allow selective cross-coupling reactions, making it valuable in constructing complex organic molecules. Commonly employed in palladium-catalyzed reactions such as Suzuki or Heck couplings to form carbon-carbon bonds. Also utilized in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Its hydroxyl group enables further derivatization, such as esterification or ether formation, enhancing its versatility in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,140.00

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(3-Bromo-2-iodophenyl)methanol
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its functional groups—bromine and iodine—allow selective cross-coupling reactions, making it valuable in constructing complex organic molecules. Commonly employed in palladium-catalyzed reactions such as Suzuki or Heck couplings to form carbon-carbon bonds. Also utilized in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Its h

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its functional groups—bromine and iodine—allow selective cross-coupling reactions, making it valuable in constructing complex organic molecules. Commonly employed in palladium-catalyzed reactions such as Suzuki or Heck couplings to form carbon-carbon bonds. Also utilized in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Its hydroxyl group enables further derivatization, such as esterification or ether formation, enhancing its versatility in medicinal chemistry research.

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