4-Methyl-7-nitro-1H-indazole

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Reagent Code: #47661
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CAS Number 104103-06-2

science Other reagents with same CAS 104103-06-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.1601 g/mol
Formula C₈H₇N₃O₂
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MDL Number MFCD08689688
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Primarily used in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is leveraged in the development of potential therapeutic agents, particularly in the field of oncology, where it may contribute to the creation of novel anti-cancer drugs. Additionally, it is explored in the study of enzyme inhibition, aiding in the understanding of biochemical pathways and the design of enzyme-targeted treatments. Its nitro and indazole groups make it a valuable component in organic synthesis, facilitating the production of complex chemical entities for further pharmacological evaluation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,368.00

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4-Methyl-7-nitro-1H-indazole
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Primarily used in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is leveraged in the development of potential therapeutic agents, particularly in the field of oncology, where it may contribute to the creation of novel anti-cancer drugs. Additionally, it is explored in the study of enzyme inhibition, aiding in the understanding of biochemical pathways and the design of enzyme-targeted treatments. Its nitro and in

Primarily used in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is leveraged in the development of potential therapeutic agents, particularly in the field of oncology, where it may contribute to the creation of novel anti-cancer drugs. Additionally, it is explored in the study of enzyme inhibition, aiding in the understanding of biochemical pathways and the design of enzyme-targeted treatments. Its nitro and indazole groups make it a valuable component in organic synthesis, facilitating the production of complex chemical entities for further pharmacological evaluation.

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