3-Iodo-1-methyl-1H-indazole-6-carboxylic acid

95%

Reagent Code: #198594
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CAS Number 1363381-70-7

science Other reagents with same CAS 1363381-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.07 g/mol
Formula C₉H₇IN₂O₂
badge Registry Numbers
MDL Number MFCD21642007
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used 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 for constructing indazole-based bioactive molecules. Its iodo and carboxylic acid functional groups allow for further derivatization through cross-coupling reactions and amide formation, making it valuable in drug discovery research. Also employed in the preparation of selective probes for biological targets due to the indazole core’s affinity for various enzymes and receptors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,000.00
1g
10-20 days ฿18,110.00
3-Iodo-1-methyl-1H-indazole-6-carboxylic acid
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Used 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 for constructing indazole-based bioactive molecules. Its iodo and carboxylic acid functional groups allow for further derivatization through cross-coupling reactions and amide formation, making it valuable in drug discovery research. Also employed in the preparation of selective probes for biological target

Used 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 for constructing indazole-based bioactive molecules. Its iodo and carboxylic acid functional groups allow for further derivatization through cross-coupling reactions and amide formation, making it valuable in drug discovery research. Also employed in the preparation of selective probes for biological targets due to the indazole core’s affinity for various enzymes and receptors.

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