Methyl 1-methyl-1H-indazole-3-carboxylate

≥95%

Reagent Code: #205556
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CAS Number 109216-60-6

science Other reagents with same CAS 109216-60-6

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scatter_plot Molecular Information
Weight 190.20 g/mol
Formula C₁₀H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD03840643
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a synthetic intermediate in the preparation of bioactive compounds, particularly in medicinal chemistry for developing analogs with potential pharmacological activity. It serves as a building block in the synthesis of indazole-based derivatives that are investigated for their use in central nervous system agents, anti-inflammatory compounds, and kinase inhibitors. Commonly employed in research settings to explore structure-activity relationships in drug discovery programs. Its ester functionality allows for further chemical modifications, enabling the introduction of various substituents to optimize biological activity and pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,280.00
inventory 5g
10-20 days ฿8,710.00

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Methyl 1-methyl-1H-indazole-3-carboxylate
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Used as a synthetic intermediate in the preparation of bioactive compounds, particularly in medicinal chemistry for developing analogs with potential pharmacological activity. It serves as a building block in the synthesis of indazole-based derivatives that are investigated for their use in central nervous system agents, anti-inflammatory compounds, and kinase inhibitors. Commonly employed in research settings to explore structure-activity relationships in drug discovery programs. Its ester functionality

Used as a synthetic intermediate in the preparation of bioactive compounds, particularly in medicinal chemistry for developing analogs with potential pharmacological activity. It serves as a building block in the synthesis of indazole-based derivatives that are investigated for their use in central nervous system agents, anti-inflammatory compounds, and kinase inhibitors. Commonly employed in research settings to explore structure-activity relationships in drug discovery programs. Its ester functionality allows for further chemical modifications, enabling the introduction of various substituents to optimize biological activity and pharmacokinetic properties.

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