4-Nitro-1H-indole-3-carbaldehyde

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Reagent Code: #218579
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CAS Number 10553-11-4

science Other reagents with same CAS 10553-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.16 g/mol
Formula C₉H₆N₂O₃
badge Registry Numbers
MDL Number MFCD04973979
thermostat Physical Properties
Melting Point 189 - 193 ℃
Boiling Point 441.47 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.517 g/cm3
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the preparation of indole-based derivatives with potential antitumor, antiviral, and antimicrobial activities. Commonly employed in the development of kinase inhibitors and fluorescent probes due to its ability to undergo selective functionalization at the aldehyde and nitro groups. Also utilized in materials science for designing organic semiconductors and optoelectronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,550.00
inventory 1g
10-20 days ฿8,240.00
inventory 5g
10-20 days ฿25,200.00
inventory 25g
10-20 days ฿88,180.00

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4-Nitro-1H-indole-3-carbaldehyde
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the preparation of indole-based derivatives with potential antitumor, antiviral, and antimicrobial activities. Commonly employed in the development of kinase inhibitors and fluorescent probes due to its ability to undergo selective functionalization at the aldehyde and nitro groups. Also utilized in materials science for designing organic semiconductors and optoelectronic materials.

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the preparation of indole-based derivatives with potential antitumor, antiviral, and antimicrobial activities. Commonly employed in the development of kinase inhibitors and fluorescent probes due to its ability to undergo selective functionalization at the aldehyde and nitro groups. Also utilized in materials science for designing organic semiconductors and optoelectronic materials.

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