3-Chloro-7-nitro-1H-indazole

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Reagent Code: #156630
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CAS Number 74209-33-9

science Other reagents with same CAS 74209-33-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.58 g/mol
Formula C₇H₄ClN₃O₂
badge Registry Numbers
MDL Number MFCD11976299
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as an 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 reactive functional groups, enabling the formation of complex heterocyclic systems. Its nitro and chloro substituents allow for selective transformations, such as reductions and cross-coupling reactions, facilitating the creation of diverse drug candidates. Also explored in research settings for developing new bioactive molecules with potential anti-inflammatory and neuroprotective properties.

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inventory 1g
10-20 days ฿3,650.00

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3-Chloro-7-nitro-1H-indazole
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Used primarily as an 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 reactive functional groups, enabling the formation of complex heterocyclic systems. Its nitro and chloro substituents allow for selective transformations, such as reductions and cross-coupling reactions, facilitating the creation of diverse drug candidates. Also explored in research settin

Used primarily as an 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 reactive functional groups, enabling the formation of complex heterocyclic systems. Its nitro and chloro substituents allow for selective transformations, such as reductions and cross-coupling reactions, facilitating the creation of diverse drug candidates. Also explored in research settings for developing new bioactive molecules with potential anti-inflammatory and neuroprotective properties.

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