1-(2-Nitrophenyl)-1H-pyrrole

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Reagent Code: #218926
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CAS Number 33265-60-0

science Other reagents with same CAS 33265-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.18 g/mol
Formula C₁₀H₈N₂O₂
badge Registry Numbers
MDL Number MFCD00047062
thermostat Physical Properties
Melting Point 58 °C
inventory_2 Storage & Handling
Density 1.23 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of complex nitrogen-containing compounds, making it valuable in constructing bioactive molecules. It is also employed in photochemistry due to the nitro group's light-sensitive properties, enabling applications in photoremovable protecting groups and molecular switches. Additionally, it serves as a building block in the synthesis of dyes and functional materials where conjugated systems with electron-withdrawing groups are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿3,230.00
inventory 5g
10-20 days ฿13,140.00

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1-(2-Nitrophenyl)-1H-pyrrole
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of complex nitrogen-containing compounds, making it valuable in constructing bioactive molecules. It is also employed in photochemistry due to the nitro group's light-sensitive properties, enabling applications in photoremovable protecting groups and molecular switches. Additionally, it serves as a building block in the synthesis of dyes and func

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of complex nitrogen-containing compounds, making it valuable in constructing bioactive molecules. It is also employed in photochemistry due to the nitro group's light-sensitive properties, enabling applications in photoremovable protecting groups and molecular switches. Additionally, it serves as a building block in the synthesis of dyes and functional materials where conjugated systems with electron-withdrawing groups are required.

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