5-Nitro-1H-indole-3-carbaldehyde

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Reagent Code: #217287
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CAS Number 6625-96-3

science Other reagents with same CAS 6625-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.16 g/mol
Formula C₉H₆N₂O₃
badge Registry Numbers
MDL Number MFCD01313781
thermostat Physical Properties
Melting Point 300°C
Boiling Point 441.5°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based drugs with biological activity. Commonly applied in the preparation of antitumor, antiviral, and antimicrobial agents due to its reactive aldehyde and nitro functional groups. Also employed in organic research for constructing complex heterocyclic systems through condensation and cyclization reactions. Its structure allows for further derivatization, making it valuable in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿270.00
inventory 1g
10-20 days ฿430.00
inventory 5g
10-20 days ฿2,090.00
inventory 25g
10-20 days ฿8,460.00

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5-Nitro-1H-indole-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based drugs with biological activity. Commonly applied in the preparation of antitumor, antiviral, and antimicrobial agents due to its reactive aldehyde and nitro functional groups. Also employed in organic research for constructing complex heterocyclic systems through condensation and cyclization reactions. Its structure allows for further derivatization, making it valuable in medicinal chemistry an

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based drugs with biological activity. Commonly applied in the preparation of antitumor, antiviral, and antimicrobial agents due to its reactive aldehyde and nitro functional groups. Also employed in organic research for constructing complex heterocyclic systems through condensation and cyclization reactions. Its structure allows for further derivatization, making it valuable in medicinal chemistry and drug discovery.

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