1-Ethyl-1H-pyrazole-5-carbaldehyde

95%

Reagent Code: #184066
label
Alias 2-ethylpyrazole-3-formaldehyde
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CAS Number 902837-62-1

science Other reagents with same CAS 902837-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.14 g/mol
Formula C₆H₈N₂O
badge Registry Numbers
MDL Number MFCD03130036
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with biological activity. Its aldehyde functional group allows for easy modification, enabling the formation of imines, oximes, or other derivatives useful in drug discovery. Commonly employed in agrochemical research for creating novel pesticides and herbicides due to the pyrazole ring’s favorable metabolic stability and binding properties. Also utilized in the preparation of functional materials and ligands for catalysis. Its versatility in cross-coupling reactions and heterocyclic elaboration makes it valuable in medicinal chemistry and combinatorial synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,180.00
inventory 1g
10-20 days ฿3,060.00
inventory 5g
10-20 days ฿10,980.00
inventory 25g
10-20 days ฿35,480.00

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1-Ethyl-1H-pyrazole-5-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with biological activity. Its aldehyde functional group allows for easy modification, enabling the formation of imines, oximes, or other derivatives useful in drug discovery. Commonly employed in agrochemical research for creating novel pesticides and herbicides due to the pyrazole ring’s favorable metabolic stability and binding properties. Also utilized in the prep

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with biological activity. Its aldehyde functional group allows for easy modification, enabling the formation of imines, oximes, or other derivatives useful in drug discovery. Commonly employed in agrochemical research for creating novel pesticides and herbicides due to the pyrazole ring’s favorable metabolic stability and binding properties. Also utilized in the preparation of functional materials and ligands for catalysis. Its versatility in cross-coupling reactions and heterocyclic elaboration makes it valuable in medicinal chemistry and combinatorial synthesis.

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