Methyl 2-(1H-indazol-4-yl)acetate

≥95%

Reagent Code: #205454
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CAS Number 1357945-60-8

science Other reagents with same CAS 1357945-60-8

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scatter_plot Molecular Information
Weight 190.20 g/mol
Formula C₁₀H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD22376776
inventory_2 Storage & Handling
Storage Room temperature

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Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Shows relevance in the production of potential anticancer agents due to the indazole core’s affinity for enzyme targets involved in cell proliferation. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates targeting inflammatory and neurological disorders. Its ester functionality allows for easy modification, making it valuable in creating derivative libraries for high-throughput screening.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,700.00
inventory 500mg
10-20 days ฿66,870.00

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Methyl 2-(1H-indazol-4-yl)acetate
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Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Shows relevance in the production of potential anticancer agents due to the indazole core’s affinity for enzyme targets involved in cell proliferation. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates targeting inflammatory and neurological disorders. Its ester functionality allows f

Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Shows relevance in the production of potential anticancer agents due to the indazole core’s affinity for enzyme targets involved in cell proliferation. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates targeting inflammatory and neurological disorders. Its ester functionality allows for easy modification, making it valuable in creating derivative libraries for high-throughput screening.

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