3-Iodo-5-methoxy-1H-indazole

98%

Reagent Code: #201033
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CAS Number 290367-99-6

science Other reagents with same CAS 290367-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.06 g/mol
Formula C₈H₇IN₂O
badge Registry Numbers
MDL Number MFCD07781661
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. The iodine substituent enables potential applications in radiolabeling for medical imaging, such as positron emission tomography (PET), where it can be replaced with radioisotopes. It shows promise in the development of kinase inhibitors, crucial for cancer therapy by regulating cell signaling pathways. Additionally, it is investigated for creating selective ligands for neurological receptors, relevant to central nervous system drug discovery. Its indazole core with methoxy and iodo substituents supports medicinal chemistry efforts to optimize potency and selectivity in small molecule drugs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,490.00
inventory 250mg
10-20 days ฿11,030.00
inventory 1g
10-20 days ฿36,500.00
3-Iodo-5-methoxy-1H-indazole
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Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. The iodine substituent enables potential applications in radiolabeling for medical imaging, such as positron emission tomography (PET), where it can be replaced with radioisotopes. It shows promise in the development of kinase inhibitors, crucial for cancer therapy by regulating cell signaling pathways. Additionally, it is investigated for creating selective ligands for neurological receptors,

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. The iodine substituent enables potential applications in radiolabeling for medical imaging, such as positron emission tomography (PET), where it can be replaced with radioisotopes. It shows promise in the development of kinase inhibitors, crucial for cancer therapy by regulating cell signaling pathways. Additionally, it is investigated for creating selective ligands for neurological receptors, relevant to central nervous system drug discovery. Its indazole core with methoxy and iodo substituents supports medicinal chemistry efforts to optimize potency and selectivity in small molecule drugs.

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