4-Methyl-7-nitro-1H-indole

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Reagent Code: #210028
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CAS Number 289483-80-3

science Other reagents with same CAS 289483-80-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.17 g/mol
Formula C₉H₈N₂O₂
badge Registry Numbers
MDL Number MFCD07780760
thermostat Physical Properties
Boiling Point 384.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, inflatable, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of biologically active molecules. Its structure supports the construction of nitrogen-containing heterocyclic systems, which are common in drugs targeting neurological and inflammatory conditions. It is also employed in research settings for the preparation of fluorescent probes and sensors due to its favorable electronic properties. In medicinal chemistry, derivatives built from this scaffold are explored for their potential anticonvulsant, antidepressant, and antimicrobial activities. Its nitro group allows for further functionalization, enabling the creation of a wide range of indole-based compounds for drug discovery and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,170.00
inventory 250mg
10-20 days ฿7,710.00
inventory 1g
10-20 days ฿26,750.00

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4-Methyl-7-nitro-1H-indole
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of biologically active molecules. Its structure supports the construction of nitrogen-containing heterocyclic systems, which are common in drugs targeting neurological and inflammatory conditions. It is also employed in research settings for the preparation of fluorescent probes and sensors due to its favorable electronic properties. In medicinal chemistry, derivatives built from this scaffold are explored for their potential anticonvulsant, antidepressant, and antimicrobial activities. Its nitro group allows for further functionalization, enabling the creation of a wide range of indole-based compounds for drug discovery and materials science.
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