N-Isopropylidene-N'-2-nitrobenzenesulfonyl hydrazine

98%

Reagent Code: #216627
label
Alias N'-isopropylene-2-nitrobenzenesulfonyl
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CAS Number 6655-27-2

science Other reagents with same CAS 6655-27-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.27 g/mol
Formula C₉H₁₁N₃O₄S
badge Registry Numbers
MDL Number MFCD09800525
thermostat Physical Properties
Melting Point 131-135 °C
Boiling Point 421.3±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.41±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of sulfonyl hydrazide derivatives which exhibit biological activity. It serves as a building block in heterocyclic chemistry, enabling the construction of nitrogen-containing rings such as pyrazoles and triazoles through cyclization reactions. Its nitro and sulfonyl groups facilitate selective transformations, making it valuable in medicinal chemistry for developing compounds with insecticidal, antifungal, or herbicidal properties. Also employed in research for designing novel organic molecules with tailored reactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿1,160.00
inventory 5g
10-20 days ฿4,110.00
inventory 50g
10-20 days ฿25,050.00
N-Isopropylidene-N'-2-nitrobenzenesulfonyl hydrazine
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of sulfonyl hydrazide derivatives which exhibit biological activity. It serves as a building block in heterocyclic chemistry, enabling the construction of nitrogen-containing rings such as pyrazoles and triazoles through cyclization reactions. Its nitro and sulfonyl groups facilitate selective transformations, making it valuable in medicinal chemistry for developing compounds with insecticida

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of sulfonyl hydrazide derivatives which exhibit biological activity. It serves as a building block in heterocyclic chemistry, enabling the construction of nitrogen-containing rings such as pyrazoles and triazoles through cyclization reactions. Its nitro and sulfonyl groups facilitate selective transformations, making it valuable in medicinal chemistry for developing compounds with insecticidal, antifungal, or herbicidal properties. Also employed in research for designing novel organic molecules with tailored reactivity.

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