(E)-2-(4-Chlorobenzylidene)hydrazine-1-carboximidamide

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Reagent Code: #180604
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CAS Number 132685-68-8

science Other reagents with same CAS 132685-68-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.64 g/mol
Formula C₈H₉ClN₄
badge Registry Numbers
MDL Number MFCD00205397
thermostat Physical Properties
Boiling Point 312.6±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiparasitic and antimicrobial agents. Its structure supports the formation of nitrogen-rich heterocycles, which are common in bioactive molecules. It also serves in agrochemical formulations for crop protection due to its stability and reactivity in condensation reactions. Additionally, it is employed in research settings for designing novel imidazole and pyridine derivatives with potential therapeutic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,240.00
inventory 5g
10-20 days ฿14,810.00

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(E)-2-(4-Chlorobenzylidene)hydrazine-1-carboximidamide
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiparasitic and antimicrobial agents. Its structure supports the formation of nitrogen-rich heterocycles, which are common in bioactive molecules. It also serves in agrochemical formulations for crop protection due to its stability and reactivity in condensation reactions. Additionally, it is employed in research settings for designing novel imidazole and pyridine derivatives with potential thera

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiparasitic and antimicrobial agents. Its structure supports the formation of nitrogen-rich heterocycles, which are common in bioactive molecules. It also serves in agrochemical formulations for crop protection due to its stability and reactivity in condensation reactions. Additionally, it is employed in research settings for designing novel imidazole and pyridine derivatives with potential therapeutic applications.

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