1-Methyl-4-(2-nitrovinyl)-1H-pyrazole

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Reagent Code: #210512
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CAS Number 3156-58-9

science Other reagents with same CAS 3156-58-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₆H₇N₃O₂
badge Registry Numbers
MDL Number MFCD16061742
thermostat Physical Properties
Boiling Point 300.1±17.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive compounds with insecticidal and fungicidal properties. Its nitrovinyl group enables Michael addition reactions, making it valuable in organic synthesis for constructing nitrogen-containing heterocycles. Also explored in the preparation of pyrazole-based derivatives for potential use in medicinal chemistry due to their activity in biological systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,050.00
inventory 250mg
10-20 days ฿3,420.00
inventory 1g
10-20 days ฿7,070.00

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1-Methyl-4-(2-nitrovinyl)-1H-pyrazole
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive compounds with insecticidal and fungicidal properties. Its nitrovinyl group enables Michael addition reactions, making it valuable in organic synthesis for constructing nitrogen-containing heterocycles. Also explored in the preparation of pyrazole-based derivatives for potential use in medicinal chemistry due to their activity in biological systems.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive compounds with insecticidal and fungicidal properties. Its nitrovinyl group enables Michael addition reactions, making it valuable in organic synthesis for constructing nitrogen-containing heterocycles. Also explored in the preparation of pyrazole-based derivatives for potential use in medicinal chemistry due to their activity in biological systems.

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