3-Ethoxy-4-iodo-1H-pyrazole

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Reagent Code: #184985
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CAS Number 1207431-89-7

science Other reagents with same CAS 1207431-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.03 g/mol
Formula C₅H₇IN₂O
badge Registry Numbers
MDL Number MFCD30002182
thermostat Physical Properties
Melting Point 114 °C
Boiling Point 341.3±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.926±0.06 g/cm3(Predicted)
Storage Room temperature, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules. Its structure allows for functionalization in heterocyclic compound design, making it valuable in medicinal chemistry for creating potential drug candidates. Also employed in research settings for the preparation of iodinated pyrazole derivatives, which are explored for their biological activity, including antifungal and anticancer properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,020.00
inventory 250mg
10-20 days ฿13,610.00
inventory 1g
10-20 days ฿30,950.00

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3-Ethoxy-4-iodo-1H-pyrazole
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules. Its structure allows for functionalization in heterocyclic compound design, making it valuable in medicinal chemistry for creating potential drug candidates. Also employed in research settings for the preparation of iodinated pyrazole derivatives, which are explored for their biological activity, including antifungal and anticancer properties.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules. Its structure allows for functionalization in heterocyclic compound design, making it valuable in medicinal chemistry for creating potential drug candidates. Also employed in research settings for the preparation of iodinated pyrazole derivatives, which are explored for their biological activity, including antifungal and anticancer properties.

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