5-Bromo-2-methyl-2H-indazole-3-carbaldehyde

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Reagent Code: #150260
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CAS Number 1251023-52-5

science Other reagents with same CAS 1251023-52-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.07 g/mol
Formula C₉H₇BrN₂O
badge Registry Numbers
MDL Number MFCD11520882
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and halogenated aromatic structure, enabling coupling reactions and heterocycle formation. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its structural features make it valuable in high-throughput screening and structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,520.00
inventory 1g
10-20 days ฿3,710.00
inventory 5g
10-20 days ฿14,970.00

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5-Bromo-2-methyl-2H-indazole-3-carbaldehyde
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and halogenated aromatic structure, enabling coupling reactions and heterocycle formation. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and halogenated aromatic structure, enabling coupling reactions and heterocycle formation. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its structural features make it valuable in high-throughput screening and structure-activity relationship (SAR) studies.

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