6-Bromo-4-fluoro-3-iodo-1H-indazole

98%

Reagent Code: #79614
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CAS Number 887568-00-5

science Other reagents with same CAS 887568-00-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340.92 g/mol
Formula C₇H₃BrFIN₂
badge Registry Numbers
MDL Number MFCD07781844
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a versatile building block for the synthesis of more complex molecules. Its structure, featuring multiple halogen substituents, makes it a valuable intermediate in the development of potential drug candidates, particularly those targeting various diseases such as cancer, inflammation, and infectious diseases. The presence of bromo, fluoro, and iodo groups allows for selective chemical modifications, enabling researchers to explore structure-activity relationships and optimize the biological activity of the final compounds. Additionally, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse indazole derivatives with potential therapeutic applications. Its role in the development of kinase inhibitors and other enzyme-targeting agents is also noteworthy, as indazole scaffolds are commonly found in biologically active molecules.

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inventory 250mg
10-20 days ฿19,233.00

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6-Bromo-4-fluoro-3-iodo-1H-indazole
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a versatile building block for the synthesis of more complex molecules. Its structure, featuring multiple halogen substituents, makes it a valuable intermediate in the development of potential drug candidates, particularly those targeting various diseases such as cancer, inflammation, and infectious diseases. The presence of bromo, fluoro, and iodo groups allows for selective chemical modifications, ena

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a versatile building block for the synthesis of more complex molecules. Its structure, featuring multiple halogen substituents, makes it a valuable intermediate in the development of potential drug candidates, particularly those targeting various diseases such as cancer, inflammation, and infectious diseases. The presence of bromo, fluoro, and iodo groups allows for selective chemical modifications, enabling researchers to explore structure-activity relationships and optimize the biological activity of the final compounds. Additionally, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse indazole derivatives with potential therapeutic applications. Its role in the development of kinase inhibitors and other enzyme-targeting agents is also noteworthy, as indazole scaffolds are commonly found in biologically active molecules.

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