3-Iodo-1H-indazol-7-amine

97%

Reagent Code: #201132
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CAS Number 1000340-82-8

science Other reagents with same CAS 1000340-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.05 g/mol
Formula C₇H₆IN₃
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MDL Number MFCD09027047
inventory_2 Storage & Handling
Storage Room temperature

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 construction of complex heterocyclic systems. Its amine and iodo functional groups allow for sequential derivatization, making it valuable in drug discovery for generating compound libraries. Also employed in research targeting neurological disorders due to the indazole core’s bioactivity profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,760.00
inventory 250mg
10-20 days ฿6,290.00
inventory 5g
10-20 days ฿42,950.00
inventory 1g
10-20 days ฿12,560.00
3-Iodo-1H-indazol-7-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 construction of complex heterocyclic systems. Its amine and iodo functional groups allow for sequential derivatization, making it valuable in drug discovery for generating compound libraries. Also employed in research targeting n

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 construction of complex heterocyclic systems. Its amine and iodo functional groups allow for sequential derivatization, making it valuable in drug discovery for generating compound libraries. Also employed in research targeting neurological disorders due to the indazole core’s bioactivity profile.

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