Methyl 5-nitro-1H-indole-3-carboxylate

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Reagent Code: #207019
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CAS Number 686747-51-3

science Other reagents with same CAS 686747-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.18 g/mol
Formula C₁₀H₈N₂O₄
badge Registry Numbers
MDL Number MFCD06204072
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry. Commonly employed in the preparation of potential drug candidates targeting neurological disorders and inflammation. Also utilized in research settings to synthesize fluorescent probes and functional materials due to the indole core’s electron-rich properties. The nitro group allows further functionalization through reduction to amino derivatives, enabling diverse chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,680.00
inventory 250mg
10-20 days ฿2,310.00
inventory 1g
10-20 days ฿7,040.00
inventory 5g
10-20 days ฿21,380.00

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Methyl 5-nitro-1H-indole-3-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry. Commonly employed in the preparation of potential drug candidates targeting neurological disorders and inflammation. Also utilized in research settings to synthesize fluorescent probes and functional materials due to the indole core’s electron-rich properties. The nitro group allows further functionalization

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry. Commonly employed in the preparation of potential drug candidates targeting neurological disorders and inflammation. Also utilized in research settings to synthesize fluorescent probes and functional materials due to the indole core’s electron-rich properties. The nitro group allows further functionalization through reduction to amino derivatives, enabling diverse chemical transformations.

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