Methyl 3-bromo-5-iodo-2-methylbenzoate

≥95%

Reagent Code: #214226
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CAS Number 1370600-52-4

science Other reagents with same CAS 1370600-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 354.97 g/mol
Formula C₉H₈BrIO₂
badge Registry Numbers
MDL Number MFCD20526667
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound enables the construction of complex aromatic structures through selective cross-coupling reactions. The presence of both bromo and iodo substituents allows for sequential functionalization using palladium-catalyzed reactions such as Suzuki or Stille couplings, making it valuable in medicinal chemistry for building substituted benzene derivatives. Its ester group can be hydrolyzed or transformed to other functional groups, further expanding its utility in drug development. Commonly employed in research settings to design bioactive molecules, particularly in the development of kinase inhibitors and anti-inflammatory agents.

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inventory 5g
10-20 days ฿54,120.00

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Methyl 3-bromo-5-iodo-2-methylbenzoate
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound enables the construction of complex aromatic structures through selective cross-coupling reactions. The presence of both bromo and iodo substituents allows for sequential functionalization using palladium-catalyzed reactions such as Suzuki or Stille couplings, making it valuable in medicinal chemistry for building substituted benzene derivatives. Its ester group can be hydrolyzed or transformed to ot

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound enables the construction of complex aromatic structures through selective cross-coupling reactions. The presence of both bromo and iodo substituents allows for sequential functionalization using palladium-catalyzed reactions such as Suzuki or Stille couplings, making it valuable in medicinal chemistry for building substituted benzene derivatives. Its ester group can be hydrolyzed or transformed to other functional groups, further expanding its utility in drug development. Commonly employed in research settings to design bioactive molecules, particularly in the development of kinase inhibitors and anti-inflammatory agents.

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