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

95%

Reagent Code: #49919
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CAS Number 885520-72-9

science Other reagents with same CAS 885520-72-9

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Weight 243.0300 g/mol
Formula C₈H₄BrFN₂O
badge Registry Numbers
MDL Number MFCD07781554
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for designing drug candidates, particularly in the fields of oncology and neurology. It is often employed in the creation of small molecule inhibitors targeting specific enzymes or receptors involved in disease pathways. Additionally, its aldehyde group allows for further functionalization, enabling chemists to develop diverse chemical libraries for high-throughput screening. This compound is also utilized in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of potential therapeutic agents.

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inventory 1g
10-20 days ฿4,986.00

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6-Bromo-4-fluoro-1H-indazole-3-carbaldehyde
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This compound is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for designing drug candidates, particularly in the fields of oncology and neurology. It is often employed in the creation of small molecule inhibitors targeting specific enzymes or receptors involved in disease pathways. Additionally, its aldehyde group all

This compound is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for designing drug candidates, particularly in the fields of oncology and neurology. It is often employed in the creation of small molecule inhibitors targeting specific enzymes or receptors involved in disease pathways. Additionally, its aldehyde group allows for further functionalization, enabling chemists to develop diverse chemical libraries for high-throughput screening. This compound is also utilized in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of potential therapeutic agents.

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