3-Iodo-1H-indazol-5-amine

98%

Reagent Code: #200516
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CAS Number 599183-36-5

science Other reagents with same CAS 599183-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.05 g/mol
Formula C₇H₆IN₃
badge Registry Numbers
MDL Number MFCD07781656
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

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 due to its ability to undergo selective cross-coupling reactions, enabling the introduction of indazole-based scaffolds into bioactive molecules. Its amino and iodo functional groups allow for sequential derivatization, making it valuable in drug discovery programs targeting inflammatory diseases and neurological disorders. Also employed in the preparation of radiolabeled compounds for use in positron emission tomography (PET) imaging studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿360.00
inventory 250mg
10-20 days ฿890.00
inventory 1g
10-20 days ฿2,380.00
3-Iodo-1H-indazol-5-amine
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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 due to its ability to undergo selective cross-coupling reactions, enabling the introduction of indazole-based scaffolds into bioactive molecules. Its amino and iodo functional groups allow for sequential derivatization, making it valuable in drug discovery programs targeting inflammatory diseases and neurol

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 due to its ability to undergo selective cross-coupling reactions, enabling the introduction of indazole-based scaffolds into bioactive molecules. Its amino and iodo functional groups allow for sequential derivatization, making it valuable in drug discovery programs targeting inflammatory diseases and neurological disorders. Also employed in the preparation of radiolabeled compounds for use in positron emission tomography (PET) imaging studies.

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