3-Iodo-1H-indazole-5-carboxylic acid

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Reagent Code: #200186
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CAS Number 885521-46-0

science Other reagents with same CAS 885521-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.04 g/mol
Formula C₈H₅IN₂O₂
badge Registry Numbers
MDL Number MFCD07781585
thermostat Physical Properties
Boiling Point 512.1°C at 760 mmHg
inventory_2 Storage & Handling
Density 2.22g/cm3
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment and bioactive molecules targeting inflammation and neurodegenerative diseases. Its indazole core enables effective interactions with biomolecular targets, while the reactive iodine site facilitates selective modifications, including iodine transfer reactions for derivatives in medical imaging and radiolabeling for diagnostics. Also employed in agrochemical research for designing new pesticides with improved efficacy and environmental safety. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its stable aromatic structure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿890.00
inventory 10g
10-20 days ฿7,030.00
inventory 25g
10-20 days ฿13,700.00
inventory 5g
10-20 days ฿3,580.00

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3-Iodo-1H-indazole-5-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 and bioactive molecules targeting inflammation and neurodegenerative diseases. Its indazole core enables effective interactions with biomolecular targets, while the reactive iodine site facilitates selective modifications, including iodine transfer reactions for derivatives in medical imaging and radiolabeling for diagnostics. Also employed in agrochemical resear
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment and bioactive molecules targeting inflammation and neurodegenerative diseases. Its indazole core enables effective interactions with biomolecular targets, while the reactive iodine site facilitates selective modifications, including iodine transfer reactions for derivatives in medical imaging and radiolabeling for diagnostics. Also employed in agrochemical research for designing new pesticides with improved efficacy and environmental safety. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its stable aromatic structure.
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