6-Chloro-4-nitro-1H-indazole

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Reagent Code: #160596
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CAS Number 885519-50-6

science Other reagents with same CAS 885519-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.58 g/mol
Formula C₇H₄ClN₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its structure supports the construction of more complex heterocyclic systems, particularly in the design of kinase inhibitors and other enzyme-targeting agents. The presence of both chloro and nitro functional groups allows for selective modifications through substitution or reduction reactions, enabling fine-tuning of molecular properties in drug discovery programs. It is also investigated for potential applications in agrochemicals due to its ability to act as a scaffold in pesticidal and herbicidal agents.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿590.00
inventory 250mg
10-20 days ฿1,440.00

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6-Chloro-4-nitro-1H-indazole
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Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its structure supports the construction of more complex heterocyclic systems, particularly in the design of kinase inhibitors and other enzyme-targeting agents. The presence of both chloro and nitro functional groups allows for selective modifications through substitution or reduction reactions, enabling fine-tuning of molecular properties in dru

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its structure supports the construction of more complex heterocyclic systems, particularly in the design of kinase inhibitors and other enzyme-targeting agents. The presence of both chloro and nitro functional groups allows for selective modifications through substitution or reduction reactions, enabling fine-tuning of molecular properties in drug discovery programs. It is also investigated for potential applications in agrochemicals due to its ability to act as a scaffold in pesticidal and herbicidal agents.

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